Job Title: Civil Structural EngineerJob DescriptionWe are seeking a Civil Structural Engineer who is dedicated to providing exceptional professional service while embracing a strong team environment. The successful candidate will possess strong written and oral communication skills, impeccable follow-through, and a passion for their work. They should enjoy project variety and problem-solving while accepting ownership and responsibility for assigned projects and tasks. Opportunities for professional growth and advancement abound in this role, though travel and fieldwork may be required for some projects.Responsibilities<ul><li>Plan and manage scope, schedule, and budget for assigned projects.</li><li>Independently perform detailed calculations for moderate to complex analyses and structural systems.</li><li>Lead and coordinate with other project team members to ensure successful completion of small to midsize projects.</li><li>Assist with mentoring less experienced engineers.</li><li>Perform site visits, collect field data, conduct research and investigations, and prepare reports.</li><li>Review contractor submittals during construction for conformance to construction document requirements.</li><li>Assist with the preparation of construction cost estimates.</li></ul>Essential Skills<ul><li>Bachelor’s degree in engineering.</li><li>0-3+ years of experience in the design of structural components and systems (industrial, marine, etc.).</li><li>Competence in the design of structural steel systems and components.</li><li>Strong work ethic and a positive attitude.</li><li>Self-starter and results-oriented.</li><li>Valid driver's license in the US.</li><li>Ability to travel periodically.</li></ul>Additional Skills &amp; Qualifications<ul><li>Currently licensed as a PE or SE.</li><li>7+ years of structural design experience.</li><li>Experience with the design of wood/timber, concrete, and masonry.</li><li>1+ years of building design experience.</li><li>Competency in using Risa 3D or Ram Elements.</li><li>Competency in using Revit.</li></ul>Work EnvironmentThe role is based in a small, unique engineering firm that is in growth mode and boasts a tremendous backlog of work from both the marine and federal industries. The firm supports the department of national parks and undertakes very unique projects. The position offers a competitive salary based on experience, along with benefits such as group health insurance, 401K with automatic distribution, term life insurance, long-term disability insurance, AD&amp;D insurance, profit-sharing bonuses, paid holidays, and a minimum of three weeks of paid personal leave.Job Type &amp; LocationThis is a Permanent position based out of Pensacola, FL.Pay and BenefitsThe pay range for this position is $38.46 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Pensacola,FL.Application DeadlineThis position is anticipated to close on Apr 8, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

public

Civil Structural Engineer

Job Title: Civil Structural EngineerJob DescriptionWe are seeking a Civil Structural Engineer who is dedicated to providing exceptional professional service while embracing a strong team environment. The successful candidate will possess strong written and oral communication skills, impeccable follow-through, and a passion for their work. They should enjoy project variety and problem-solving while accepting ownership and responsibility for assigned projects and tasks. Opportunities for professional growth and advancement abound in this role, though travel and fieldwork may be required for some projects.Responsibilities<ul><li>Plan and manage scope, schedule, and budget for assigned projects.</li><li>Independently perform detailed calculations for moderate to complex analyses and structural systems.</li><li>Lead and coordinate with other project team members to ensure successful completion of small to midsize projects.</li><li>Assist with mentoring less experienced engineers.</li><li>Perform site visits, collect field data, conduct research and investigations, and prepare reports.</li><li>Review contractor submittals during construction for conformance to construction document requirements.</li><li>Assist with the preparation of construction cost estimates.</li></ul>Essential Skills<ul><li>Bachelor’s degree in engineering.</li><li>0-3+ years of experience in the design of structural components and systems (industrial, marine, etc.).</li><li>Competence in the design of structural steel systems and components.</li><li>Strong work ethic and a positive attitude.</li><li>Self-starter and results-oriented.</li><li>Valid driver's license in the US.</li><li>Ability to travel periodically.</li></ul>Additional Skills &amp; Qualifications<ul><li>Currently licensed as a PE or SE.</li><li> structural design experience.</li><li>Experience with the design of wood/timber, concrete, and masonry.</li><li>1+ years of building design experience.</li><li>Competency in using Risa 3D or Ram Elements.</li><li>Competency in using Revit.</li></ul>Work EnvironmentThe role is based in a small, unique engineering firm that is in growth mode and boasts a tremendous backlog of work from both the marine and federal industries. The firm supports the department of national parks and undertakes very unique projects. The position offers a competitive salary based on experience, along with benefits such as group health insurance, 401K with automatic distribution, term life insurance, long-term disability insurance, AD&amp;D insurance, profit-sharing bonuses, paid holidays, and a minimum of three weeks of paid personal leave.Job Type &amp; LocationThis is a Contract to Hire position based out of Pensacola, FL.Pay and BenefitsThe pay range for this position is $38.46 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Pensacola,FL.Application DeadlineThis position is anticipated to close on Apr 15, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Civil Structural EngineerJob DescriptionWe are seeking a Civil Structural Engineer who is dedicated to providing exceptional professional service while embracing a strong team environment. The successful candidate will possess strong written and oral communication skills, impeccable follow-through, and a passion for their work. They should enjoy project variety and problem-solving while accepting ownership and responsibility for assigned projects and tasks. Opportunities for professional growth and advancement abound in this role, though travel and fieldwork may be required for some projects.Responsibilities<ul><li>Plan and manage scope, schedule, and budget for assigned projects.</li><li>Independently perform detailed calculations for moderate to complex analyses and structural systems.</li><li>Lead and coordinate with other project team members to ensure successful completion of small to midsize projects.</li><li>Assist with mentoring less experienced engineers.</li><li>Perform site visits, collect field data, conduct research and investigations, and prepare reports.</li><li>Review contractor submittals during construction for conformance to construction document requirements.</li><li>Assist with the preparation of construction cost estimates.</li></ul>Essential Skills<ul><li>Bachelor’s degree in engineering.</li><li>0-3+ years of experience in the design of structural components and systems (industrial, marine, etc.).</li><li>Competence in the design of structural steel systems and components.</li><li>Strong work ethic and a positive attitude.</li><li>Self-starter and results-oriented.</li><li>Valid driver's license in the US.</li><li>Ability to travel periodically.</li></ul>Additional Skills &amp; Qualifications<ul><li>Currently licensed as a PE or SE.</li><li>7+ years of structural design experience.</li><li>Experience with the design of wood/timber, concrete, and masonry.</li><li>1+ years of building design experience.</li><li>Competency in using Risa 3D or Ram Elements.</li><li>Competency in using Revit.</li></ul>Work EnvironmentThe role is based in a small, unique engineering firm that is in growth mode and boasts a tremendous backlog of work from both the marine and federal industries. The firm supports the department of national parks and undertakes very unique projects. The position offers a competitive salary based on experience, along with benefits such as group health insurance, 401K with automatic distribution, term life insurance, long-term disability insurance, AD&amp;D insurance, profit-sharing bonuses, paid holidays, and a minimum of three weeks of paid personal leave.Job Type &amp; LocationThis is a Contract to Hire position based out of Pensacola, FL.Pay and BenefitsThe pay range for this position is $38.46 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Pensacola,FL.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Civil Superintendent for Data Center projectsJob DescriptionThe Project Superintendent will manage and control assigned projects, including overseeing field operations, site safety, productivity, schedule, and quality of work. The role involves working closely with contractors, suppliers, and the Project Manager. The Superintendent directs and supervises activities of workers engaged in the construction process and coordinates various phases of construction to prevent delays. A thorough understanding of safety hazards related to the work and the ability to safely use or operate work-related tools and equipment is essential. The position requires working in a plant operations or construction jobsite setting.Responsibilities<ul><li>Manage and control assigned projects, ensuring field operations are efficient.</li><li>Oversee site safety, productivity, schedule, and quality of work.</li><li>Work closely with contractors, suppliers, and Project Manager.</li><li>Direct and supervise activities of workers engaged in the construction process.</li><li>Coordinate various phases of construction to prevent delays.</li><li>Learn and understand all safety hazards related to the work.</li><li>Safely and effectively use or operate work-related tools and equipment.</li></ul>Essential Skills<ul><li>Civil construction oversight</li><li>Site development</li><li>5+ years of Civil Superintendent experience for large CAPEX projects</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with data centers, LNG, and petrochemical CAPEX projects</li></ul>Work EnvironmentThe work environment includes data centers, LNG, and petrochemical CAPEX projects. The role requires working in plant operations or construction jobsite settings. Company truck, per diem provided.Job Type &amp; LocationThis is a Permanent position based out of Baton Rouge, LA.Pay and BenefitsThe pay range for this position is $90000.00 - $150000.00/yr.Healthcare 
Dental
Vision
401KWorkplace TypeThis is a fully onsite position in Baton Rouge,LA.Application DeadlineThis position is anticipated to close on Apr 14, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Civil Superintendent

Position SummaryActalent connects passion with purpose. We are supporting critical engineering and sciences initiatives that advance how companies serve the world. With almost 40 years of experience, our scalable talent solutions and engineering and sciences services provide the expertise our customers need to achieve more.The position falls within the transmission department of the organization. The engineer will be working with senior engineers to complete projects that support our utility customer. They will work with in-house and client engineers and designers.Primary Duties and Responsibilities<ul><li>Responsible for the engineering and design activities related to transmission line design such as engineering analysis and design, route selection, material acquisition, structural and foundation design, and project and construction management with the guidance of higher level engineers</li><li>Become familiar with preparing project construction documents such as: plan and profile drawings; design drawings; engineering, material, and construction specifications; project schedules and bills of material</li><li>Help develop project design alternatives and corresponding cost estimates with assistance of higher level engineers</li><li>Learn to design new transmission facilities with voltages ranging from 69kV and 765kV</li><li>Utilize PLS-CADD to model transmission line design project</li><li>Work under supervision of Transmission II, III, IV, and senior Engineers</li><li>Position will require occasional site visits</li></ul>Education and Experience Requirements<ul><li>Zero to two years of experience in utilities working with Transmission Line Design</li><li>Zero to two years of experience completing engineering projects from start to finish</li><li>Zero to two years of experience scoping, estimating, and ordering materials for Transmission Lines projects</li><li>Bachelor’s Degree in Civil Engineering or Electrical Engineering (ABET)</li><li>Master’s Degree in Civil Engineering or Electrical Engineering (ABET) will count toward years of experience</li><li>An EIT License is desirable but not required</li></ul>Requisite Abilities and Skills<ul><li>Work effectively with both internal and external customers, including Project Management, Substation Design, Distribution, Supply Chain and Right-of-Way</li><li>Possess excellent verbal and written communication skills to facilitate adhering to project schedule and budget</li><li>Familiarity with standards and codes such as IEEE, ANSI, NEC and NESC</li><li>Demonstrate ability to work with others in supplying information and seeking assistance as necessary</li><li>Demonstrate willingness and capabilities to assume leadership roles</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Roanoke, VA.Pay and BenefitsThe pay range for this position is $28.85 - $36.06/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Roanoke,VA.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Civil/Structural Engineer I

<h2 style="text-align:center;">Civil CAD Technician – Municipal Water/Wastewater</h2>Interested in learning more? Directly apply to Chaney Cornell with your most up-to-date resume to chcornell@actalentservices .comA civil engineering consulting firm specializing in municipal water and wastewater infrastructure is seeking a Civil CAD Technician to support the production of construction drawings for public infrastructure projects. This role offers long-term stability within a recession-resistant industry and the opportunity to contribute to essential public systems.The Civil CAD Technician will work closely with engineers and project managers, providing hands-on drafting support using AutoCAD and Civil 3D.KEY RESPONSIBILITIES<ul><li>Produce civil construction drawings using AutoCAD and Civil 3D</li><li>Prepare plan sets, profiles, details, and design exhibits</li><li>Support engineers and project managers throughout the design process</li><li>Assist with quantity take-offs and design coordination</li><li>Participate in occasional site visits or field verification, as needed</li><li>Contribute to a collaborative and team-oriented drafting environment</li></ul>WHY THIS OPPORTUNITY STANDS OUT<ul><li>Variety of drafting work across multiple disciplines, including civil, architectural, structural, MEP, and process piping, providing broad technical exposure and preventing repetitive, single-discipline work</li><li>Intentional focus on training and professional development, with clear job title tiers, skill progression, and corresponding pay tiers</li><li>Use of modern technology to support internal training and productivity, including structured learning tools and systems</li><li>Cross-training opportunities across multiple software platforms and workflows to support long-term skill growth</li><li>CAD-led reporting structure, with the CAD team reporting to dedicated CAD leadership rather than engineering management</li><li>Leadership team that is highly invested in the CAD profession, drafting standards, and evolving design technology</li><li>Continued investment in advanced visualization tools, including virtual reality and virtual walk-through software used to support client presentations and project communication</li><li>Supportive, collaborative engineering culture with a consistent project workload</li><li>Competitive compensation benchmarked in the top 10–15% of the market</li><li>Annual performance reviews and merit-based compensation increases</li></ul>QUALIFICATIONS<ul><li>Experience using AutoCAD and Civil 3D in a professional setting</li><li>Familiarity with civil construction drawings and plan production</li><li>Exposure to municipal, utility, roadway, or site development projects preferred</li><li>Strong attention to detail and ability to collaborate within a design team</li></ul>Candidates who value technical variety, intentional career development, and CAD-focused leadership within a stable municipal infrastructure environment are encouraged to inquire.Job Type &amp; LocationThis is a Permanent position based out of Indianapolis, IN.Pay and BenefitsThe pay range for this position is $32.50 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Indianapolis,IN.Application DeadlineThis position is anticipated to close on Apr 15, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Civil3D CAD Technician

Description
					The Cleaning Validation Specialist is responsible for the execution and documentation of cleaning validation activities for laboratory equipment within a GMP-regulated contract development and manufacturing organization (CDMO). This role supports established cleaning validation programs by performing sampling, data collection, and protocol adherence to ensure equipment cleanliness and regulatory compliance.

Key Responsibilities:
Execute approved cleaning validation protocols, including swab and rinse sampling activities
Collect, review, and accurately document validation data in compliance with GMP and data integrity requirements
Perform visual inspections and verify equipment readiness following cleaning activities
Support equipment changeovers, routine revalidation, and continued process verification activities
Assist with deviation investigations related to cleaning execution and support CAPA implementation
Maintain validation records and support document updates as needed
					 					Skills
					hplc instrumentation
					 					Top Skills Details
					hplc instrumentation
					 					Additional Skills &amp; Qualifications
					Bachelor’s degree in a scientific or technical discipline
3+ years experience performing cleaning validation activities in a GMP manufacturing environment
Familiarity with swab/rinse sampling techniques and GMP documentation practices
Strong attention to detail and ability to follow approved procedures and protocols
					 					Experience Level
					Intermediate Level
					 Job Type &amp; LocationThis is a Contract position based out of Verona, WI.Pay and BenefitsThe pay range for this position is $30.00 - $32.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Verona,WI.Application DeadlineThis position is anticipated to close on Apr 17, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleaning Validation Specialist

<h2>Cleanroom Technician - Research &amp; Development</h2>Long-Term Opportunity | Day Shift: M-F | Offers Benefits Job DescriptionWe are seeking a diligent Cleanroom Technician to join our team in a clean room manufacturing environment focused on creating biological medical devices derived from porcine liver. Your primary role will involve handling and processing porcine livers, ensuring that they meet the highest standards of quality and safety.Responsibilities<ul><li>Receive and trim porcine livers.</li><li>Scoop and mix solutions for liver processing.</li><li>Decellularize porcine livers.</li><li>Create and cut specific pieces for medical devices.</li><li>Sterilize the clean room to maintain a safe working environment.</li><li>Follow Standard Operating Procedures (SOPs) meticulously.</li></ul>Requirements<ul><li>6+ months of experience working within a clean room setting </li><li>Experience following SOPs in GMP environment</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Plymouth,MN.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleanroom Technician

Job Title: Cleanroom Technician Job DescriptionJoin our team as a Cleanroom Technician, working in a state-of-the-art clean room manufacturing environment. You will be part of an innovative team focused on creating biological medical devices derived from porcine liver. Your role will involve critical processes such as receiving, trimming, and preparing porcine livers, as well as ensuring a sterile environment for these operations.Responsibilities<ul><li>Receive and trim porcine livers for processing.</li><li>Scoop and mix solutions for liver preparation.</li><li>Decellurize porcine livers following established protocols.</li><li>Create and cut specific pieces for medical devices.</li><li>Sterilize and maintain the clean room environment.</li><li>Adhere to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).</li></ul>Essential Skills<ul><li>Experience working in a clean room setting for at least 6 months.</li><li>Proficiency in sterile processing and aseptic techniques.</li><li>Ability to follow SOPs in a GMP environment.</li><li>Strong attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with cleanroom operations and sterilization processes.</li><li>Background in chemistry or biology is advantageous.</li><li>Experience working with tissue samples, particularly porcine or animal tissue, is a bonus.</li><li>Reliable and hardworking with a positive attitude.</li><li>Ability to lift up to 25lbs.</li></ul>Work EnvironmentThe role involves working directly with porcine livers and occasionally assisting with research and development involving porcine kidneys. The work environment is wet, and technicians are required to regularly lift weights up to 25lbs. The work schedule varies with decell weeks typically running Monday from 8 AM to 4:30 PM, Tuesday to Thursday from 6 AM to 3:30 PM, and Friday from 6 AM to noon or until 40 hours are completed. Packaging and non-decell weeks follow a standard Monday to Friday schedule from 8 AM to 4:30 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in plymouth,MN.Application DeadlineThis position is anticipated to close on Apr 16, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleanroom TechnicianJob DescriptionJoin our team as a Cleanroom Technician, working in a state-of-the-art clean room manufacturing environment. You will be part of an innovative team focused on creating biological medical devices derived from porcine liver. Your role will involve critical processes such as receiving, trimming, and preparing porcine livers, as well as ensuring a sterile environment for these operations.Responsibilities<ul><li>Receive and trim porcine livers for processing.</li><li>Scoop and mix solutions for liver preparation.</li><li>Decellurize porcine livers following established protocols.</li><li>Create and cut specific pieces for medical devices.</li><li>Sterilize and maintain the clean room environment.</li><li>Adhere to Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP).</li></ul>Essential Skills<ul><li>Experience working in a clean room setting for at least 6 months.</li><li>Proficiency in sterile processing and aseptic techniques.</li><li>Ability to follow SOPs in a GMP environment.</li><li>Strong attention to detail.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with cleanroom operations and sterilization processes.</li><li>Experience working with tissue samples, particularly porcine or animal tissue, is a bonus.</li><li>Reliable and hardworking with a positive attitude.</li><li>Ability to lift up to 25lbs.</li></ul>Work EnvironmentThe role involves working directly with porcine livers and occasionally assisting with research and development involving porcine kidneys. The work environment is wet, and technicians are required to regularly lift weights up to 25lbs. The work schedule varies with decell weeks typically running Monday from 8 AM to 4:30 PM, Tuesday to Thursday from 6 AM to 3:30 PM, and Friday from 6 AM to noon or until 40 hours are completed. Packaging and non-decell weeks follow a standard Monday to Friday schedule from 8 AM to 4:30 PM.Job Type &amp; LocationThis is a Contract to Hire position based out of plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in plymouth,MN.Application DeadlineThis position is anticipated to close on Apr 17, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleanroom TechnicianJob DescriptionWe are seeking a diligent Cleanroom Technician to join our team in a clean room manufacturing environment focused on creating biological medical devices derived from porcine liver. Your primary role will involve handling and processing porcine livers, ensuring that they meet the highest standards of quality and safety.Responsibilities<ul><li>Receive and trim porcine livers.</li><li>Scoop and mix solutions for liver processing.</li><li>Decellularize porcine livers.</li><li>Create and cut specific pieces for medical devices.</li><li>Sterilize the clean room to maintain a safe working environment.</li><li>Follow Standard Operating Procedures (SOPs) meticulously.</li></ul>Essential Skills<ul><li>Experience working in a cleanroom setting for at least 6 months.</li><li>Proficiency in sterile processing and aseptic techniques.</li><li>Ability to lift up to 25 lbs.</li><li>Reliability and a strong work ethic.</li></ul>Requirements- 6+ months of experience working within a clean room setting - Experience following SOPs in GMP environmentWork EnvironmentThe role involves working directly with porcine livers and occasionally assisting R&amp;D with porcine kidneys. Expect a wet environment with regular lifting of 25 lbs. The production timeline runs from Monday to the following Tuesday when products are shipped out. Production weeks require over 40 hours per week, with non-production weeks around 36 hours. During non-build weeks, the schedule is Monday to Friday, 8am-4:30pm. Build weeks vary with longer hours and some mandatory overtime, up to 44 hours.Job Type &amp; LocationThis is a Contract to Hire position based out of plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in plymouth,MN.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleanroom Technician (Biotech)

<h2>Cleanroom Technician - Research &amp; Development</h2>Long-Term Opportunity | Day Shift: M-F | Offers Benefits Job DescriptionWe are seeking a diligent Cleanroom Technician to join our team in a clean room manufacturing environment focused on creating biological medical devices derived from porcine liver. Your primary role will involve handling and processing porcine livers, ensuring that they meet the highest standards of quality and safety.Responsibilities<ul><li>Receive and trim porcine livers.</li><li>Scoop and mix solutions for liver processing.</li><li>Decellularize porcine livers.</li><li>Create and cut specific pieces for medical devices.</li><li>Sterilize the clean room to maintain a safe working environment.</li><li>Follow Standard Operating Procedures (SOPs) meticulously.</li></ul>Requirements<ul><li>Experience following written instructions in a fast-paced environment</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Plymouth, MN.Pay and BenefitsThe pay range for this position is $21.00 - $21.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Plymouth,MN.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cleanroom Technician (Entry-Level, No Degree Req)

Job Title: Clinical Contracts SpecialistJob DescriptionWe are seeking a detail-oriented and adaptable Clinical Contracts Specialist to manage contracts with CRO partners, sites, and vendors. This role involves drafting, negotiating, and managing various agreements to support clinical development and R&amp;D activities under the supervision of attorneys.Responsibilities<ul><li>Draft, negotiate, and manage a wide variety of agreements, including clinical trial agreements, confidentiality agreements, consulting and services agreements, research agreements, and material transfer agreements.</li><li>Assist with contract interpretation, compliance questions, and issue resolution under the supervision of attorneys.</li><li>Identify and assess legal and business risks associated with clinical and R&amp;D contracts, communicating these risks clearly to attorneys and internal stakeholders.</li><li>Collaborate with cross-functional internal clients, such as Clinical Operations, Research, Finance, and Procurement, to support contracting objectives and timelines.</li><li>Maintain contract records, track contract status, and support contract lifecycle management processes.</li><li>Handle miscellaneous legal and administrative tasks as needed in support of the Legal Department.</li><li>Provide general support to in-house attorneys on clinical, R&amp;D, and related contracting matters.</li></ul>Essential Skills<ul><li>Excellent attention to detail and organizational skills.</li><li>Ability to learn and adapt quickly.</li><li>Experience in writing, drafting, and negotiating clinical trial agreements both domestically and globally.</li><li>Experience managing contracts with CRO partners, sites, and vendors.</li><li>Strong negotiation skills.</li><li>Thorough understanding of the contract management process, including tracking, negotiation, approval, and signature processes.</li><li>Working knowledge of the drug discovery and development process.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA degree in a related discipline with 10 years of related experience preferred.</li><li>Ability to work independently and across various functional groups and management levels.</li><li>Knowledge of paralegal support tasks, particularly in intellectual property or corporate matters, preferred.</li><li>Strong computer skills, including Microsoft Word, Excel, and PowerPoint.</li><li>Clear and concise verbal and written communication skills.</li><li>Excellent interpersonal communication skills.</li></ul>Work EnvironmentThe position offers a dynamic work environment with some flexibility in working hours. The role requires strong computer skills and effective communication across various functional groups.Onsite 5 days a week in AlamedaJob Type &amp; LocationThis is a Contract position based out of Alameda, CA.Pay and BenefitsThe pay range for this position is $50.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Alameda,CA.Application DeadlineThis position is anticipated to close on Apr 16, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Contracts Manager

Job Title: Clinical Contracts SpecialistJob DescriptionWe are seeking a detail-oriented and adaptable Clinical Contracts Specialist to manage contracts with CRO partners, sites, and vendors. This role involves drafting, negotiating, and managing various agreements to support clinical development and R&amp;D activities under the supervision of attorneys.Responsibilities<ul><li>Draft, negotiate, and manage a wide variety of agreements, including clinical trial agreements, confidentiality agreements, consulting and services agreements, research agreements, and material transfer agreements.</li><li>Assist with contract interpretation, compliance questions, and issue resolution under the supervision of attorneys.</li><li>Identify and assess legal and business risks associated with clinical and R&amp;D contracts, communicating these risks clearly to attorneys and internal stakeholders.</li><li>Collaborate with cross-functional internal clients, such as Clinical Operations, Research, Finance, and Procurement, to support contracting objectives and timelines.</li><li>Maintain contract records, track contract status, and support contract lifecycle management processes.</li><li>Handle miscellaneous legal and administrative tasks as needed in support of the Legal Department.</li><li>Provide general support to in-house attorneys on clinical, R&amp;D, and related contracting matters.</li></ul>Essential Skills<ul><li>Excellent attention to detail and organizational skills.</li><li>Ability to learn and adapt quickly.</li><li>Experience in writing, drafting, and negotiating clinical trial agreements both domestically and globally.</li><li>Experience managing contracts with CRO partners, sites, and vendors.</li><li>Strong negotiation skills.</li><li>Thorough understanding of the contract management process, including tracking, negotiation, approval, and signature processes.</li><li>Working knowledge of the drug discovery and development process.</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA degree in a related discipline with 10 years of related experience preferred.</li><li>Ability to work independently and across various functional groups and management levels.</li><li>Knowledge of paralegal support tasks, particularly in intellectual property or corporate matters, preferred.</li><li>Strong computer skills, including Microsoft Word, Excel, and PowerPoint.</li><li>Clear and concise verbal and written communication skills.</li><li>Excellent interpersonal communication skills.</li></ul>Work EnvironmentThe position offers a dynamic work environment with some flexibility in working hours. The role requires strong computer skills and effective communication across various functional groups.Onsite 5 days a week in AlamedaJob Type &amp; LocationThis is a Contract position based out of Alameda, CA.Pay and BenefitsThe pay range for this position is $50.00 - $65.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Alameda,CA.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

The Clinical Laboratory Associate is responsible for specimen processing, test performance, and reporting test results to supervisors or directors. The role requires performing high complexity tests authorized by the laboratory director, demanding a degree of skill aligned with the individual's education, training, or experience.Responsibilities<ul><li>Follow laboratory procedures for specimen handling and processing, test analyses, reporting, and maintaining records of patient test results.</li><li>Maintain records that demonstrate proficiency testing samples are tested in the same manner as patient specimens.</li><li>Adhere to quality control policies, document all quality control activities, instrument and procedural calibrations, and maintenance performed.</li><li>Follow established policies and procedures whenever test systems are not within acceptable levels of performance.</li><li>Identify problems that may adversely affect test performance or reporting of test results and either correct the problems or notify the appropriate supervisor or director.</li><li>Document all corrective actions taken when test systems deviate from established performance specifications.</li><li>Perform statistical analysis and review of quality control testing data.</li><li>Demonstrate expertise with Microsoft Word, PowerPoint, Excel, Outlook, and equipment software.</li></ul>Essential Skills<ul><li>Specimen processing</li><li>Quality control</li><li>Verification of Assays</li><li>Pipetting</li><li>Chemistry</li><li>CLIA/CAP</li><li>Inspection</li><li>ELISA</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in medical technology, clinical laboratory, chemical, physical, or biological sciences.</li><li>Associate degree in chemical, physical, or biological science or medical laboratory or equivalent education and training.</li><li>60 semester hours or equivalent from an accredited institution including medical laboratory technology or science courses.</li><li>Completion of a clinical laboratory training program approved by ABHES, NAACLS, or similar organizations.</li><li>At least three months of documented laboratory training in each specialty for high complexity testing.</li><li>Ability to perform accessioning without direct supervision with independent verification of manual data entries.</li><li>Competence in testing without direct supervision with independent review of assay acceptance criteria.</li><li>Ability to enter test results without direct supervision with independent verification of manual data entries.</li></ul>Work EnvironmentThe work environment offers a small company, start-up feel with about 25 employees, providing innovation and agility with the security and financial backing of a parent company. The lab associates have opportunities for career growth into R&amp;D projects, including verification of assays and product development. Core working hours are Monday to Friday from 9am to 3pm, with shifts typically covering either 9am to 5pm or 10am to 6pm. The position will report to a supervisor and requires covering the end of the day due to instrument capacity.Job Type &amp; LocationThis is a Contract to Hire position based out of Broomfield, CO.Pay and BenefitsThe pay range for this position is $24.04 - $27.40/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Broomfield,CO.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Laboratory Associate

Job Title: Clinical Laboratory ScientistJob DescriptionWe are seeking a dedicated Clinical Laboratory Scientist to join our team. This role involves performing essential duties required by CLIA/CAP, including specimen processing, test performance, and reporting of test results. You will conduct routine qualitative and quantitative analyses of various clinical specimens, such as blood and urine, and maintain comprehensive records of laboratory results, quality control data, and laboratory procedures.Responsibilities<ul><li>Perform duties required by CLIA/CAP.</li><li>Responsible for specimen processing, test performance, and reporting test results.</li><li>Conduct routine qualitative and quantitative analysis of clinical specimens including blood and urine.</li><li>Maintain records of laboratory results, quality control data, and laboratory procedures.</li><li>Perform and optimize NGS library preparation on clinical samples.</li><li>Collect data as required by the SOP.</li><li>Maintain effective communication with supervisor on day-to-day activities and ongoing experiments.</li><li>Coordinate with internal and external audits and report instances of noncompliance to compliance personnel.</li><li>Perform other administrative duties as assigned.</li></ul>Essential Skills<ul><li>Proficiency in immunoassay, laboratory practices, and molecular biology.</li><li>Experience in hematology, clinical laboratory, and microbiology.</li><li>CLS Generalist license.</li><li>Experience with Beckman DxHs, Sysmex CS2500’s, Siemens Atellicas and a Siemens Centaur</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor or Master of Science Degree in Clinical Laboratory Science (Generalist).</li><li>1-3 years of experience in the biotechnology or biomedical field.</li><li>Open to entry-level CLS with a Generalist license.</li></ul>Work EnvironmentThe position operates on a shift from 2:00 PM to 10:30 PM, requiring full availability on weekends. The role involves working in a laboratory environment, utilizing state-of-the-art equipment and maintaining a professional dress code in compliance with safety standards.Job Type &amp; LocationThis is a Contract to Hire position based out of Thousand Oaks, CA.Pay and BenefitsThe pay range for this position is $42.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Thousand Oaks,CA.Application DeadlineThis position is anticipated to close on Apr 17, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Laboratory Scientist

<h2>Clinical Laboratory Technician</h2>Job DescriptionJoin a dynamic team at the Central Clinical Lab and Clinical Specialty Laboratory, where you will perform a variety of highly automated and manual testing to aid in the diagnosis and treatment of patients. This role involves working with advanced technologies in a fast-paced environment, contributing to the lab's impressive annual volume of over 5.5 million tests.Responsibilities<ul><li>Perform analyses on blood, tissue, and body fluids to assist healthcare providers in diagnosing, prognosing, and treating patients.</li><li>Operate and maintain laboratory instruments, troubleshoot assay issues, and evaluate tests for accuracy.</li><li>Assist in interpreting test results and provide operational support to optimize testing processes.</li><li>Utilize multiple computer systems to retrieve information and report results.</li><li>Adhere to safety protocols when handling infectious specimens, chemicals, and other hazards.</li><li>Participate in research studies related to new clinical tests, assessing clinical utility and outcomes.</li></ul>Essential Skills<ul><li>Experience with operation and troubleshooting of laboratory instrumentation and assay systems.</li><li>Ability to produce accurate results under time constraints and perform multitasking in a fast-paced environment.</li><li>Strong communication skills and ability to work closely with others.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in chemistry or a human biological science (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Neuroscience, etc).</li></ul>Work EnvironmentThe position involves working night shifts from 10:00pm to 6:30am, Saturday through Wednesday, or a 7-on, 7-off schedule from 8:30pm to 7:00am. The lab uses advanced technologies, including mass spectrometry, nuclear magnetic resonance, ELISA, and chromatography systems. The environment is fast-paced, with a focus on safety and efficiency.Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, MN.Pay and BenefitsThe pay range for this position is $23.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Rochester,MN.Application DeadlineThis position is anticipated to close on Apr 15, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Laboratory Technician

<h2>Clinical Laboratory Technician</h2>Job DescriptionJoin a dynamic team at the Central Clinical Lab and Clinical Specialty Laboratory, where you will perform a variety of highly automated and manual testing to aid in the diagnosis and treatment of patients. This role involves working with advanced technologies in a fast-paced environment, contributing to the lab's impressive annual volume of over 5.5 million tests.Responsibilities<ul><li>Perform analyses on blood, tissue, and body fluids to assist healthcare providers in diagnosing, prognosing, and treating patients.</li><li>Operate and maintain laboratory instruments, troubleshoot assay issues, and evaluate tests for accuracy.</li><li>Assist in interpreting test results and provide operational support to optimize testing processes.</li><li>Utilize multiple computer systems to retrieve information and report results.</li><li>Adhere to safety protocols when handling infectious specimens, chemicals, and other hazards.</li><li>Participate in research studies related to new clinical tests, assessing clinical utility and outcomes.</li></ul>Essential Skills<ul><li>Experience with operation and troubleshooting of laboratory instrumentation and assay systems.</li><li>Ability to produce accurate results under time constraints and perform multitasking in a fast-paced environment.</li><li>Strong communication skills and ability to work closely with others.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in chemistry or a human biological science (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Neuroscience, etc).</li></ul>Work EnvironmentThe position involves working night shifts from 10:00pm to 6:30am, Saturday through Wednesday, or a 7-on, 7-off schedule from 8:30pm to 7:00am. The lab uses advanced technologies, including mass spectrometry, nuclear magnetic resonance, ELISA, and chromatography systems. The environment is fast-paced, with a focus on safety and efficiency.Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, MN.Pay and BenefitsThe pay range for this position is $23.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Rochester,MN.Application DeadlineThis position is anticipated to close on Apr 17, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

<h2>Clinical Laboratory Technician</h2>Job DescriptionJoin a dynamic team at the Central Clinical Lab and Clinical Specialty Laboratory, where you will perform a variety of highly automated and manual testing to aid in the diagnosis and treatment of patients. This role involves working with advanced technologies in a fast-paced environment, contributing to the lab's impressive annual volume of over 5.5 million tests.Responsibilities<ul><li>Perform analyses on blood, tissue, and body fluids to assist healthcare providers in diagnosing, prognosing, and treating patients.</li><li>Operate and maintain laboratory instruments, troubleshoot assay issues, and evaluate tests for accuracy.</li><li>Assist in interpreting test results and provide operational support to optimize testing processes.</li><li>Utilize multiple computer systems to retrieve information and report results.</li><li>Adhere to safety protocols when handling infectious specimens, chemicals, and other hazards.</li><li>Participate in research studies related to new clinical tests, assessing clinical utility and outcomes.</li></ul>Essential Skills<ul><li>Experience with operation and troubleshooting of laboratory instrumentation and assay systems.</li><li>Ability to produce accurate results under time constraints and perform multitasking in a fast-paced environment.</li><li>Strong communication skills and ability to work closely with others.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in chemistry or a human biological science (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Neuroscience, etc).</li></ul>Work EnvironmentThe position involves working night shifts from 10:00pm to 6:30am, Saturday through Wednesday, or a 7-on, 7-off schedule from 8:30pm to 7:00am. The lab uses advanced technologies, including mass spectrometry, nuclear magnetic resonance, ELISA, and chromatography systems. The environment is fast-paced, with a focus on safety and efficiency.Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, MN.Pay and BenefitsThe pay range for this position is $23.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Rochester,MN.Application DeadlineThis position is anticipated to close on Apr 7, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Laboratory Technician (Entry-Level)

Job Title: Clinical ManagerJob DescriptionThe Clinical Manager is responsible and accountable for the clinical patient treatment and support for Adult outpatient services. This role involves overseeing daily operations, ensuring compliance with accrediting and regulatory organizations, and providing leadership to clinical staff.Responsibilities<ul><li>Develop, implement, and monitor policies, procedures, goals, and objectives.</li><li>Evaluate training and performance needs of staff, recruit and select staff, conduct attendance reviews, performance evaluations, and provide managerial representation during HR investigations and disciplinary/grievance hearings.</li><li>Review referrals to ensure appropriateness of admission.</li><li>Facilitate meetings with contracted providers to address issues and improve program functioning and client outcomes.</li><li>Participate in case conferences and other meetings aimed at addressing placement/disposition challenges and identifying placement and/or treatment options.</li><li>Assist in developing strategies for improving, reviewing, and monitoring client care.</li><li>Oversee assigned clinical staff, clinical individual &amp; group sessions, and all levels of care.</li><li>Provide treatment to patients and maintain a caseload.</li><li>Ensure that all client files documentation is complete and thorough and in compliance with DPH, Joint Commission, and contract standards.</li><li>Ensure compliance in all contracts and outcomes are met or exceeded.</li><li>Oversee and monitor clinic quality assurance systems.</li><li>Responsible for accreditation activities; DPH and Joint Commission as it relates to clinical protocols.</li><li>Ensure financial benchmarks are achieved as outlined in the yearly budget.</li><li>Track data and clinician productivity and provide support to staff to ensure compliance with identified benchmarks.</li><li>Perform duties of Clinicians as required.</li><li>Manage staff schedule to ensure clinical services meet client needs.</li><li>Communicate with management staff regarding relevant program issues.</li><li>Act as liaison between VP and reporting departments.</li><li>Assure positive communication between reporting departments and other CRT departments.</li><li>Oversee, provide, and/or assure representation of CRT to and among outside agencies, community organizations, groups, and individuals.</li><li>Enhance and develop best practice treatment programs to assure continuous quality improvement for all adult programming and services.</li><li>May serve as agency liaison with external regulatory, Clinical Support planning and advisory groups, and other regulatory and service agencies.</li></ul>Essential Skills<ul><li>Clinical operation and management skills.</li><li>Case work and clinical documentation.</li><li>Proficiency in Microsoft Office.</li><li>Clinical data and chart review.</li><li>Care management and community outreach.</li><li>Regulatory compliance and quality assurance.</li><li>Budget management and EHR systems.</li><li>Training development and data tracking.</li><li>Program management and clinical supervision.</li></ul>Additional Skills &amp; Qualifications<ul><li>Master's degree in Social Work is required.</li><li>Minimum of 5 years of related clinical experience with Adult services, mental health or co-occurring Homelessness, Substance use disorders.</li><li>Minimum of 3 years’ experience in a supervisory capacity or a combination of experience equivalent to 5 years is required.</li><li>Active Certification in good standing in: Licensed Clinician Social Worker (LCSW) is required.</li><li>Demonstrated ability to work in collaboration with other service providers.</li><li>Ability to communicate effectively, compile written reports, and maintain/review case files.</li><li>Ability to supervise and motivate clinical staff to perform their duties efficiently.</li><li>Time management skills and must be computer literate.</li><li>Experience working in a JC accredited, fee-for-service environment required.</li><li>Proven experience in managerial position.</li><li>Experience in clinical supervision and program management.</li><li>Excellent knowledge of standards and regulations for the clinical field as it relates to Adult outpatient services.</li><li>Proficient in MS Office and computer systems (e.g. Electronic health records).</li><li>Knowledge of contractual compliance, clinical policy and procedures, managing clinical staff, and clinical individual &amp; group sessions specific to Adults.</li><li>Bilingual: Spanish Fluent – Speak/Written.</li></ul>Work EnvironmentTasks involve sedentary to light work, involving some reaching, handling, fingering, and/or feeling of objects and materials. Some tasks require visual perception and discrimination and oral communications ability. Tasks are regularly performed with exposure to adverse environmental conditions, such as dirt, dust, pollen, odors, wetness, humidity, rain, fumes, temperature and noise extremes, machinery, vibrations, electric currents, traffic hazards, animals/wildlife, toxic/poisonous agents, violence, disease, or pathogenic substances.Job Type &amp; LocationThis is a Contract to Hire position based out of Hartford, CT.Pay and BenefitsThe pay range for this position is $39.00 - $41.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Hartford,CT.Application DeadlineThis position is anticipated to close on Apr 9, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Manager

<h2>Clinical Medical Assistant </h2>Full‑time | Clinical Setting | Growth Opportunity in HealthcareWe are seeking a detail‑oriented Medical Assistant to join our fast‑paced medical team. This role offers excellent hands‑on clinical exposure, making it a strong stepping‑stone for individuals looking to build a long‑term career in healthcare!<h3>What You’ll Do</h3><ul><li>Document physician visits and patient encounters in the EMR system</li><li>Assist physicians with medical instruments and clinical procedures</li><li>Complete patient work‑ups after consultations</li><li>Communicate treatment plans and procedures clearly to patients</li><li>Support overall clinic flow and provide high‑quality patient care</li></ul><h3>What We’re Looking For</h3><ul><li>Associate’s or Bachelor’s degree in a life science or related field</li><li>Experience in medical assisting, patient care, or a clinical environment preferred</li><li>Strong understanding of medical terminology</li><li>Ability to multitask and thrive in a high‑volume setting</li><li>Excellent communication and patient‑facing skills</li><li>Ophthalmology or optometry experience is a plus</li><li>Bilingual skills welcome but not required</li></ul><h3>Why Join Us?</h3>This position offers meaningful patient interaction, direct exposure to physicians, and experience with clinical procedures and workflows. It’s an ideal opportunity for individuals looking to grow within the medical field and gain the type of experience valued across healthcare specialties.Job Type &amp; LocationThis is a Contract to Hire position based out of San Antonio, TX.Pay and BenefitsThe pay range for this position is $17.50 - $19.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in San Antonio,TX.Application DeadlineThis position is anticipated to close on Apr 15, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Medical Assistant

Clinical Pharmacist – Oncology SpecialtyWorkplace Type: 100% Remote<h3>About the Role</h3>We are seeking a licensed Clinical Pharmacist with experience in specialty and/or oncology pharmacy to join our team in a fully remote capacity. This role is responsible for the safe and accurate dispensing of specialty medications while providing clinical consultation to patients and healthcare providers. The pharmacist will also oversee pharmacy staff and ensure compliance with all regulatory and quality standards.<hr><h3>Key Responsibilities</h3><ul><li>Accurately fill, verify, and dispense prescribed pharmaceuticals and compounds</li><li>Provide clinical consultation and medication guidance to patients and healthcare providers</li><li>Supervise and provide oversight to pharmacy caseworkers, technicians, assistants, and support staff</li><li>Ensure prescription pricing accuracy and confirm appropriate payment methods are established</li><li>Coordinate delivery of prescriptions to the appropriate site per patient request, regulatory requirements, and cold-chain protocols</li><li>Maintain compliance with Standard Operating Procedures (SOPs), state and federal regulations, and accreditation standards</li><li>Submit and manage Adverse Events (AE) and Product Quality Complaints (PQC) as required</li><li>Support quality assurance, safety initiatives, and continuous process improvements</li></ul><hr><h3>Required Qualifications</h3><ul><li>Bachelor of Pharmacy (BPharm) or Doctor of Pharmacy (PharmD)</li><li>Active Washington State Pharmacist License (in good standing)</li><li>2+ years of experience in a specialty pharmacy or similar clinical setting</li><li>Experience with oncology medications and specialty drug workflows</li><li>Strong attention to detail and commitment to patient safety</li></ul><hr><h3>Preferred / Nice-to-Have Qualifications</h3><ul><li>Prior remote pharmacy work experience</li><li>Oncology or specialty pharmacy certification</li><li>Experience supervising pharmacy staff</li><li>Familiarity with cold-chain medication delivery and specialty pharmacy compliance</li></ul>Job Type &amp; LocationThis is a Contract position based out of Seattle, WA.Pay and BenefitsThe pay range for this position is $50.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Pharmacist (Remote)

Job Title: Clinical Pharmacist – Hematology/Oncology &amp; BMT SpecialistJob DescriptionThe Clinical Pharmacist – Hematology/Oncology &amp; BMT Specialist serves as a medication-therapy expert for the Hematology/Oncology and Stem Cell Transplant (BMT) programs. This role involves designing, managing, monitoring, verifying, and dispensing drug therapies such as chemotherapy, cellular therapy, immunotherapy, and transplant-support medications. The specialist collaborates across inpatient and outpatient services, oversees pharmacy technician and intern staff, ensures compliance with medication-management standards, and supports hospital-wide pharmacy operations.Responsibilities<ul><li>Optimize medication therapy for hematopoietic cell transplant, CAR-T, and bone marrow transplant patients, including assessment, design, and adjustment of individualized treatment plans.</li><li>Participate in daily rounds with ACGT, Oncology Infusion, and Inpatient Hematology/Oncology services and maintain continuous monitoring of assigned patients through chart review and interdisciplinary communication.</li><li>Provide ongoing medication therapy monitoring by reviewing charts, communicating with the healthcare team and families, and identifying or resolving drug-therapy problems.</li><li>Develop, implement, and maintain evidence-based protocols, chemotherapy regimens, and treatment pathways in collaboration with multidisciplinary teams and in alignment with clinical guidelines.</li><li>Utilize the facility formulary to promote safe, cost-effective care and provide patient or caregiver medication counseling as needed.</li><li>Serve as a subject matter expert in hematopoietic cell transplant pharmacotherapy, including CAR-T and BMT treatments.</li><li>Collaborate with the ACGT Medical Director to achieve and maintain FACT accreditation.</li><li>Manage daily pharmacy workflow across units, verify and evaluate medication orders, and supervise pharmacy staff.</li><li>Ensure adherence to pharmacy SOPs and medication-safety standards to mitigate risk to patients and staff.</li><li>Mentor and train pharmacy staff in oncology, BMT, and CAR-T pharmacy practice.</li><li>Document clinical interventions and maintain compliance with drug control regulations.</li><li>Conduct monthly inspections of medication storage and preparation areas.</li></ul>Essential Skills<ul><li>BS degree in Pharmacy.</li><li>Active State of Connecticut Pharmacist License.</li><li>3 years of experience in hematology/oncology or equivalent.</li><li>Comprehensive understanding of medications, including indications, dosing, monitoring, contraindications, and interactions.</li><li>Proficiency in EHR systems and oncology pharmacy systems (e.g., DoseEdge, Omnicell).</li><li>Strong critical-thinking and problem-solving skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>PharmD preferred.</li><li>Experience as a Hospital Pharmacist.</li><li>Completion of PGY1 Pharmacy Practice Residency.</li><li>Completion of PGY2 Pediatric Pharmacy Practice Residency.</li><li>Board certification in area of specialty preferred.</li><li>Advanced training/certification in area of specialty preferred.</li><li>Demonstrated expertise in hematology/oncology and bone marrow transplant pharmacotherapy.</li></ul>Work EnvironmentThe work environment is within a hospital setting, focusing on pediatric care and specialized medicine. The position involves interdisciplinary collaboration, adherence to safety standards, and regulatory compliance. The role requires effective management of competing demands and fostering a patient-centric atmosphere.Job Type &amp; LocationThis is a Permanent position based out of Hartford, CT.Pay and BenefitsThe pay range for this position is $113000.00 - $175000.00/yr.medical, vision ,dental, 401kWorkplace TypeThis is a fully onsite position in Hartford,CT.Application DeadlineThis position is anticipated to close on Apr 16, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Pharmacist – Hematology/Oncology

DescriptionRater Responsibilities: Raters are needed after guided journey activities for assessments, not for the full dosing session, typically a few hours per visit.This rater position is for psychedelic studies.Rater experience is the most crucial requirement, with backgrounds varying from medical assistants and nurses to teachers; specific education or certifications are not yet strictly defined but certified raters are preferred. sitting with patients, conducting assessments, and turning real-world symptoms into data that helps determine whether new treatments are working.SkillsClinical trial, rating scales, behavioral interview, behavioral health, psychometric testing software, clinical researchTop Skills DetailsClinical trial,rating scales,behavioral interview,behavioral health,psychometric testing software,clinical researchAdditional Skills &amp; QualificationsRating Scales: Diagnostic and Structured Assessment-MINI -Structured diagnostic interview for psychiatric disordersPsychosis and General Psychiatric Symptoms-BPRS (Brief Psychiatric Rating Scale)Dissociation and Perceptual Disturbances-CADSS (Clinician Administered Dissociative States Scale)Global Clinical Impression- CGI-I (Clinical Global Impression Improvement)- CGI-S (Clinical Global Impression Severity)Suicide Risk and Safety- C-SSRS (Columbia Suicide Severity Rating Scale)Depression- MADRS (Montgomery Åsberg Depression Rating Scale)- QIDS-SR 16 (Quick Inventory of Depressive Symptomatology Self Report)Anxiety- GAD-7 (Generalized Anxiety Disorder 7 item scale)Mania and Mood Elevation- YMRS (Y oung Mania Rating Scale)Aggression, Irritability, and Behavioral Activation- MOAA/S (Modified Overt Aggression Scale)Cognition and Processing Speed- DSST (Digit Symbol Substitution Test)Trauma and Stress Related Symptoms-PWC-20-Commonly used for post trauma or stress related symptom burdenTreatment Satisfaction and Subjective Experience-SETS (Systematic Evaluation of Treatment Emergent Symptoms)-MGH-ATRQ (MGH Antidepressant Treatment Response Questionnaire)-Often used to capture treatment response and subjective change over timeExperience LevelIntermediate LevelJob Type &amp; LocationThis is a Contract position based out of Redding, CA.Pay and BenefitsThe pay range for this position is $30.00 - $100.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Redding,CA.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Rater

Job Title: Clinical RaterJob DescriptionThis role involves working with individuals diagnosed with acute psychiatric conditions such as schizophrenia, bipolar disorder, PTSD, OCD, anxiety, and depression. The Clinical Rater will be responsible for conducting various clinical and neurocognitive test evaluations and interviews, as well as scoring tests to assess cognitive, neuropsychological, behavioral, and emotional states in accordance with study protocols.Responsibilities<ul><li>Perform interviews and ratings on study subjects to assess current levels of functioning and create a clinical impression of their psychiatric state throughout the study.</li><li>Administer neurocognitive battery tests to subjects with different CNS indications.</li><li>Complete clinical intake forms, including psychiatric history, and submit them to the study team as specified.</li><li>Assess and complete subject eligibility/screening forms and interact with the medical monitor regarding subject inquiries.</li><li>Conduct telephone screens and pre-screen potential study candidates.</li><li>Adhere to policies and principles of confidentiality, informed consent, and study subject rights.</li><li>Follow the principles of Good Clinical Practices and general ethical guidelines related to clinical trials.</li><li>Become familiar with FDA regulations pertaining to clinical trials.</li><li>Review medical history with CRC information obtained at screening and reconcile medical records, preparing PI notes to explain discrepancies if needed.</li><li>Complete Study Guides and Study Launch with CRC.</li><li>Assist the team in the management and assessment of adverse events to ensure the safety of subjects.</li><li>Assist with recruitment efforts and mentor staff as needed.</li><li>Perform other duties and responsibilities as assigned.</li></ul>Essential Skills<ul><li>Clinical assessment skills, with a PsyD or PhD in Clinical Psychology and experience in performing psychological evaluations.</li><li>Experience with acute psychiatric diagnoses such as schizophrenia, depression, anxiety, etc.</li><li>Proficiency in psychological evaluations and clinical assessments.</li></ul>Additional Skills &amp; Qualifications<ul><li>Doctorate in Clinical Psychology (Ph.D./Psy.D.) or an equivalent degree.</li><li>Open to candidates with a Master's degree or foreign medical graduates with over 10 years of clinical rating experience for clinical research.</li><li>Clinical research experience is not mandatory.</li></ul>Work EnvironmentThe position is based in Hollywood, FL with a schedule of Monday to Friday from 8 AM to 5 PM, and includes on-call duties on weekends on a rotating schedule approximately once a month. Candidates must have flexibility for weekend shifts. The role involves handling anywhere from 3 to 7 studies, depending on the number of patients per study, and seeing 1 to 7 patients per day based on the type of scales used. When not seeing patients, responsibilities include writing reports, following up with patients, and updating PIsJob Type &amp; LocationThis is a Permanent position based out of Hollywood, FL.Pay and BenefitsThe pay range for this position is $70000.00 - $115000.00/yr.Benefits package available.
Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, &amp; Christmas.Workplace TypeThis is a fully onsite position in Hollywood,FL.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Assistant﻿Job DescriptionWe are seeking a dedicated Clinical Research Assistant for a part-time position in Sioux Falls, SD. This role is a 6-month contract with the potential for extension, offering a flexible schedule of 24 hours per week. The primary focus will be assisting with data entry and administrative tasks supporting clinical trials.Responsibilities<ul><li>Verify and/or correct research study information on source documents.</li><li>Research queries and variances and provide feedback to the site data collector.</li><li>Input research study data into the trial Electronic Data Capture system, ensuring quality control for content, accuracy, and completeness.</li><li>Prepare and maintain research study files.</li><li>Compile, collate, and submit study information within established deadlines.</li><li>Assist in maintenance of regulatory documentation.</li><li>Schedule subject visits and generate appropriate reports and documents for research subjects prior to visits.</li><li>Input visit data into the Clinical Trial Management System (CTMS) to track patient visits and procedures completed against the study budget.</li><li>Process required lab specimens, label vials, and accurately fill out requisitions for storage and/or shipment per the study protocol and packaging and shipment regulations.</li><li>Perform various administrative support functions such as reception, office organization, and office supply management.</li></ul>Essential Skills<ul><li>Basic knowledge of clinical trials.</li><li>In-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules.</li><li>Basic knowledge of medical terminology.</li><li>Proficiency in MS Windows and Office applications such as Access, Outlook, Excel, and Word.</li><li>Excellent interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Knowledge of IRB communications and submissions.</li><li>Experience in patient recruitment and communication.</li><li>Familiarity with protocol design for prescreening eligible patients.</li><li>Tech-savvy with the ability to update study portals and manage administrative tasks.</li><li>Experience with oncology, clinical research, EMR, data management, and document handling.</li><li>BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting (e.g., clinical research coordinator, nurse, medical assistant).</li></ul>Work EnvironmentThe position is office-based with a typical part-time schedule of 24 hours per week, potentially on Mondays, Thursdays, and either Tuesdays or Wednesdays. The role involves engaging in patient education, community outreach, upkeep of the regulatory binder, and processing and shipment of labs while maintaining study supplies.Job Type &amp; LocationThis is a Contract position based out of Sioux Falls, SD.Pay and BenefitsThe pay range for this position is $33.00 - $34.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Sioux Falls,SD.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Assistant

Job Title: Clinical Research Assistant, TXJob DescriptionThis role involves active participation in recruitment and pre-screening events, often at various locations, to identify potential participants for clinical research. The position requires engaging with potential participants by reviewing medical records, conducting phone screenings, and obtaining informed consent. You will be responsible for scheduling participant visits, collecting and processing specimens, and ensuring data accuracy in compliance with FDA regulations and ICH guidelines. Administrative support, inventory management, and maintaining effective relationships with study participants and research personnel are also key aspects of this role.Responsibilities<ul><li>Participate in recruitment and pre-screening events.</li><li>Assist with preparation of outreach materials and recruitment of new participants.</li><li>Conduct phone screenings and request medical records of research participants.</li><li>Schedule visits and contact participants with reminders.</li><li>Obtain informed consent per SOP, under the direction of the CRC.</li><li>Complete visit procedures as required by protocol.</li><li>Collect, process, and ship specimens as directed by protocol.</li><li>Record data legibly and enter in real-time on paper or e-source documents.</li><li>Request study participant payments and update internal trackers.</li><li>Assist with query resolution and administrative tasks such as copying, scanning, filing, and mailing.</li><li>Maintain all site logs and manage inventory and ordering of equipment and supplies.</li><li>Ensure adherence to FDA regulations and ICH guidelines.</li><li>Foster effective relationships with study participants, research personnel, and sponsor representatives.</li><li>Communicate clearly both verbally and in writing.</li><li>Perform other duties as assigned, representative of the nature and level of work.</li></ul>Required Skills &amp; Experience<ul><li>A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant, or Phlebotomist.</li><li>Phlebotomy experience is required.</li><li>Strong communication skills and professionalism.</li><li>Excellent organizational skills with attention to detail.</li><li>A working knowledge of medical and research terminology.</li><li>Understanding of federal regulations and Good Clinical Practices (GCP).</li><li>Critical thinking and problem-solving abilities.</li><li>Proficiency in Microsoft Office Suite.</li></ul>Work EnvironmentThe position is based in an on-site clinic environment, requiring interaction with patients, sponsor representatives, and team members in a professional setting.Job Type &amp; LocationThis is a Contract position based out of Tyler, TX.Pay and BenefitsThe pay range for this position is $25.00 - $30.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Tyler,TX.Application DeadlineThis position is anticipated to close on Apr 7, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Assistant - Tyler, TX

Job Title: Clinical Research Coordinator﻿﻿Job DescriptionWe are seeking a dedicated Clinical Research Coordinator to join a prestigious research institute. In this role, you will play a vital part in coordinating clinical trials. Your primary responsibilities will include recruiting, screening, and enrolling subjects into clinical trials, as well as explaining the informed consent process. You will also be responsible for documenting adverse events and preparing Institutional Review Board (IRB) applications.Responsibilities<ul><li>Recruit, screen, and enroll subjects into clinical trials.</li><li>Explain the informed consent process to participants.</li><li>Document any adverse events that occur during the study.</li><li>Collect and manage study documents, protocols, regulatory documents, informed consents, case report forms, and source documents.</li><li>Prepare and submit applications to the Institutional Review Board (IRB).</li></ul>Required Skills<ul><li>BA/BS degree required.</li><li>1-3 years of clinical research experience required.</li><li>Experience with in-hospital clinical research.</li><li>Proficiency in patient recruitment and consenting.</li><li>Effective communication and writing skills.</li><li>Knowledge of IRB and human research protection regulations.</li><li>Experience with adverse event reporting.</li><li>Understanding of Good Clinical Practice (GCP) and Electronic Data Capture (EDC) systems.</li></ul>Work EnvironmentThe position involves working in a combination of office and hospital/outpatient surgery settings. You will be part of a fast-paced and high-volume environment, handling industry and investigator studies. The role is based on a large campus and involves working with state-of-the-art equipment. This opportunity allows you to collaborate on high-profile studies with large, well-known sponsors. The team is part of one of the most prestigious academic research institutes in the world.Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $25.00 - $31.25/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Coordinator

Job Title: Clinical Research Coordinator﻿Job DescriptionThis position provides support for the coordination and execution of research studies conducted at the Medical Center. <ul><li>Key responsibilities include assisting with participant recruitment and enrollment, facilitating grant-related activities, collecting research data, and supporting overall study operations. </li><li>The role also serves as a point of contact for the Institutional Review Board (IRB), the Research on Decedents Oversight Committee, and both internal and external funding agencies.</li><li>The coordinator helps ensure that all research activities are carried out in compliance with Good Clinical Practices (GCP), HIPAA regulations, and all other relevant requirements protecting patients, subjects, decedents, investigators, and research sponsors. </li><li>The role involves direct interaction with patients, study participants, and Principal Investigators, particularly in support of clinical trials. This position operates under general supervision.</li></ul>Qualifications<ul><li>Bachelor’s degree in life sciences, allied health, or a related field, or an equivalent combination of education and experience </li><li>2 years of clinical research experience</li><li>Proficiency in Microsoft Office applications (Word, Excel, Access, PowerPoint, Outlook).</li><li>Phlebotomy experience preferred</li></ul>Job Type &amp; LocationThis is a Contract position based out of Maryville, IL.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Maryville,IL.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator to join our team. The successful candidate will play a crucial role in overseeing and executing various clinical studies, ensuring compliance with Good Clinical Practice (GCP) guidelines and protocols. This position offers a dynamic work environment where you will be responsible for managing study documentation, coordinating study visits, and ensuring the efficient execution of clinical research projects.Responsibilities<ul><li>Serve as the lead coordinator on clinical studies, ensuring all aspects of the study are executed efficiently.</li><li>Conduct follow-up visits for ongoing studies and resolve queries specific to the study.</li><li>Perform daily tasks such as document review, data entry, test material preparation, and data collection.</li><li>Coordinate and execute projects assigned by the Clinic Manager, adhering to GCP guidelines.</li><li>Perform station and instrumentation duties, including the collection and recording of clinical information.</li><li>Respond to queries from the Quality Assurance and Statistics departments.</li><li>Set up and conduct studies in compliance with protocol, SOPs, applicable regulations, and GCPs.</li><li>Prepare for and conduct pre-study meetings and other relevant meetings and processes.</li><li>Monitor compliance of panelists with study protocols.</li><li>Prepare and manage test materials for studies, ensuring adherence to the study budget.</li><li>Complete, organize, and maintain study documentation, including drafting protocol amendments and case report forms.</li><li>Ensure staff working on managed studies understand and perform duties according to protocol, SOPs, and GCPs.</li><li>Coordinate scheduling of subjects for study visits.</li><li>Perform additional duties or tasks as assigned by the Clinic Manager and/or Supervisor.</li></ul>Essential Skills<ul><li>Bachelor's degree in Science, preferably with science experience.</li><li>Understanding of basic concepts in clinical research.</li><li>Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Outgoing, team-oriented, and customer service-oriented.</li><li>Organized and proactive, with a willingness to hit the ground running.</li><li>Knowledge of GMP/GLP/GCP standards.</li><li>Experience working on efficacy and hydration studies, as well as handwashing studies, is beneficial but not required.</li></ul>Work EnvironmentThe role involves working in a clinic setting on efficacy and hydration studies, as well as in a micro setting on handwashing studies. The position is part of a third-party cosmetics testing environment, which demands a professional and adaptable approach. The hours are usually M-F 8a-5p but depending on the study you may have to work a 12 hour day or on the weekends. You will need to be flexible with your hours for the study. Job Type &amp; LocationThis is a Contract to Hire position based out of Phoenix, AZ.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Phoenix,AZ.Application DeadlineThis position is anticipated to close on Apr 17, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Descriptionusually assign studies by sponsor11-15 studies per coordinatorwill see 20-25 patients per weekThe Clinical Research Coordinator leads and manages clinical trials in compliance with regulatory standards, working closely with the investigative team, pharmaceutical sponsors, and research participants. This role requires a strong medical background, proficiency in Good Clinical Practices (GCP), FDA regulations, and a commitment to ethical research standards. KEY RESPONSIBILITIES: Duties will include, but are not limited to:• Manage and oversee the execution of clinical trials under the direction of the Principal Investigator and Site Manager.• Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring.• Administer questionnaires, diaries, and other participant materials as per protocol.• Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met.• Maintain accurate case report forms, cross-referencing patient medical records for completeness and FDA compliance.• Collect, enter, and manage clinical data while maintaining confidentiality.• Monitor study participants, ensuring adherence to study guidelines and ethical standards.• Manage investigational medications, including receiving, dispensing, and performing drug accountability.• Collaborate with laboratories to process, ship, and ensure review of investigational reports.• Actively participate in recruiting and screening study participants.• Maintain organized records of study materials, ensuring all regulatory documentation is up to date.• Ensure necessary supplies and equipment are available and functional for each study.• Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services.Skillsclinical research, bilingual, bilingual proficiency skills, phlebotomy, phlebotomy certification, phlebotomy certifiedTop Skills Detailsclinical researchAdditional Skills &amp; QualificationsSOFT SKILLSgood bedside mannermust have a back bone!the PI is very direct, so must be able to take feedbackbasic social skills - want patients to feel comfortable and confidentproblem solving skillsEDUCATION REQUIREMENTS:• High School Diploma or GED • Preferred: Bachelor’s or Master’s degree in a related field.EXPERIENCE:• Required: Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines.• Preferred: Certification as a Clinical Research Coordinator (CCRC).Experience LevelIntermediate LevelJob Type &amp; LocationThis is a Contract position based out of Fountain Valley, CA.Pay and BenefitsThe pay range for this position is $28.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Fountain Valley,CA.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

DescriptionThe Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB. This position is directly responsible to ensure that all documentation is timely and accurate and works closely with the PI to ensure strict compliance to study protocols (GCP/ICH).Duties:• Reads and understands all correspondence relating to each study assigned. Responsible for all written and verbal communication and the documentation thereof. This will include but not be limited to communications with study sponsors, monitors, study subjects/patients, physicians and laboratories or other study-specified service providers.• Responsible for all IP accountability specific to each subject and total protocol inventory. Role includes proper documentation of IP assignment, temperature and expiration date monitoring, return of used IP, and destruction or return to sponsor.• Works with subjects/patients to ensure study compliance and understanding of participation requirements (i.e., timeliness of visits, return of study-related materials and at-home documentation.• Complete, accurate and timely entry (within 7 days of visit) of visit data into study electronic data capture sites when applicable.• Recruits and retains study Participants.• Processes, packages, and ships biological samples as required by study or centralized laboratories.• Organizes and maintains study binders for each participant in a study. Ensures that filing is complete, accurate and consistent among study participants.• Attends investigators’ meetings as required.• Works with patients to ensure that study requirements are met including appointments, labs, etc.• Networks and researches potential new studies.• Performs regulatory functions for existing studies.• Maintains control over study medications/supplies.Additional Skills &amp; QualificationsMinimum 2 years experience in a clinical research setting where they actually manage patients - consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data. Not looking for someone with only experience in data trials (or device trials as just confirmed by Helen). Must have Oncology Experience in a Clinical SettingStrong computer skills – eg Knowledge of EPIC, Outlook, MS Teams, Word, ExcelExperience LevelIntermediate Level<ul><li>This posting is for an existing vacancy.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Anaheim, CA.Pay and BenefitsThe pay range for this position is $33.00 - $42.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Anaheim,CA.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator to support study coordination, patient recruitment, and enrollment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work under close supervision within a specific Division, directly collaborating with study physicians, research coordinators, project managers, and other research staff to advance our research mission.Responsibilities<ul><li>Assist with study coordination and recruitment for various research projects.</li><li>Conduct screening visits and consent participants for studies.</li><li>Process and ship laboratory samples.</li><li>Enter data into databases accurately and promptly.</li><li>Escort participants to other testing or procedure areas.</li></ul>Essential Skills<ul><li>Experience in clinical research, patient enrollment, and recruitment.</li><li>Strong data entry skills.</li><li>Familiarity with chart review, GCP, pre-screening patients, IRB, and EDC.</li></ul>Additional Skills &amp; Qualifications<ul><li>1-2 years of related experience or an equivalent combination of education and experience.</li></ul>Work EnvironmentThis role offers WFH flexibility with the first week on-site, 1 day WFH for the first 4 months, and 2 days WFH once established, provided it does not interfere with essential duties. The work environment is supportive, with a diverse and collaborative team. The position is located near center city, with convenient access to public transportation, and there is parking available nearby. The Department of Neurology provides comprehensive evaluation, diagnosis, treatment, and management for movement disorders, and the work is both fulfilling and impactful.Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $24.00 - $26.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Apr 7, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Coordinator (Contract Position)Contract Duration: Until December 2026Schedule: 30 hours per week, Monday–Friday during standard business hoursLocation: OnsiteStart Date: ASAPPosition OverviewWe are seeking a detail‑oriented and proactive Clinical Research Coordinator (CRC) to support an ongoing clinical trial. The ideal candidate has hands-on clinical research experience, strong organizational skills, and the ability to engage confidently with participants and research staff. Key ResponsibilitiesParticipant Recruitment &amp; Screening<ul><li>Identify, recruit, and prescreen potential participants for eligibility.</li><li>Conduct phone screenings and review inclusion/exclusion criteria.</li><li>Perform thorough reviews of patient medical records to determine suitability.</li><li>Build and maintain relationships with referral physicians to support recruitment.</li></ul>Data &amp; Documentation Management<ul><li>Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy.</li><li>Resolve EDC data queries promptly.</li><li>Retrieve necessary medical records and ensure proper documentation.</li></ul>QualificationsClinical Research Experience: Previous experience as a Clinical Research Coordinator is required.Technical Proficiency: Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.Communication Skills: Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members.Attention to Detail: Demonstrated accuracy in documentation, data entry, and protocol adherence.Job Type &amp; LocationThis is a Contract position based out of Leesburg, VA.Pay and BenefitsThe pay range for this position is $25.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Leesburg,VA.Application DeadlineThis position is anticipated to close on Apr 15, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator to join our team. The successful candidate will play a crucial role in overseeing and executing various clinical studies, ensuring compliance with Good Clinical Practice (GCP) guidelines and protocols. This position offers a dynamic work environment where you will be responsible for managing study documentation, coordinating study visits, and ensuring the efficient execution of clinical research projects.Responsibilities<ul><li>Serve as the lead coordinator on clinical studies, ensuring all aspects of the study are executed efficiently.</li><li>Conduct follow-up visits for ongoing studies and resolve queries specific to the study.</li><li>Perform daily tasks such as document review, data entry, test material preparation, and data collection.</li><li>Coordinate and execute projects assigned by the Clinic Manager, adhering to GCP guidelines.</li><li>Perform station and instrumentation duties, including the collection and recording of clinical information.</li><li>Respond to queries from the Quality Assurance and Statistics departments.</li><li>Set up and conduct studies in compliance with protocol, SOPs, applicable regulations, and GCPs.</li><li>Prepare for and conduct pre-study meetings and other relevant meetings and processes.</li><li>Monitor compliance of panelists with study protocols.</li><li>Prepare and manage test materials for studies, ensuring adherence to the study budget.</li><li>Complete, organize, and maintain study documentation, including drafting protocol amendments and case report forms.</li><li>Ensure staff working on managed studies understand and perform duties according to protocol, SOPs, and GCPs.</li><li>Coordinate scheduling of subjects for study visits.</li><li>Perform additional duties or tasks as assigned by the Clinic Manager and/or Supervisor.</li></ul>Essential Skills<ul><li>Bachelor's degree in Science, preferably with a background in science.</li><li>Understanding of basic concepts in clinical research.</li><li>Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Outgoing, team-oriented, and customer service-oriented.</li><li>Organized and proactive, with a willingness to hit the ground running.</li><li>Knowledge of GMP/GLP/GCP standards.</li><li>Experience working on efficacy and hydration studies, as well as handwashing studies, is beneficial but not required.</li></ul>Work EnvironmentThe role involves working in a clinic setting on efficacy and hydration studies, as well as in a micro setting on handwashing studies. The position is part of a third-party cosmetics testing environment, which demands a professional and adaptable approach. The hours are usually M-F 8a-5p but depending on the study you may have to work a 12 hour day or on the weekends. You will need to be flexible with your hours for the study. Job Type &amp; LocationThis is a Contract to Hire position based out of Phoenix, AZ.Pay and BenefitsThe pay range for this position is $22.00 - $22.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Phoenix,AZ.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Coordinator﻿﻿Job DescriptionWe are seeking a dedicated Clinical Research Coordinator to join a prestigious research institute. In this role, you will play a vital part in coordinating clinical trials. Your primary responsibilities will include recruiting, screening, and enrolling subjects into clinical trials, as well as explaining the informed consent process. You will also be responsible for documenting adverse events and preparing Institutional Review Board (IRB) applications.Responsibilities<ul><li>Recruit, screen, and enroll subjects into clinical trials.</li><li>Explain the informed consent process to participants.</li><li>Document any adverse events that occur during the study.</li><li>Collect and manage study documents, protocols, regulatory documents, informed consents, case report forms, and source documents.</li><li>Prepare and submit applications to the Institutional Review Board (IRB).</li></ul>Essential Skills<ul><li>1-3 years of clinical research experience required.</li><li>Experience with in-hospital clinical research.</li><li>Proficiency in patient recruitment and consenting.</li><li>Effective communication and writing skills.</li><li>Knowledge of IRB and human research protection regulations.</li><li>Experience with adverse event reporting.</li><li>Understanding of Good Clinical Practice (GCP) and Electronic Data Capture (EDC) systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>BA/BS degree preferred.</li></ul>Work EnvironmentThe position involves working in a combination of office and hospital/outpatient surgery settings. You will be part of a fast-paced and high-volume environment, handling industry and investigator studies. The role is based on a large campus and involves working with state-of-the-art equipment. This opportunity allows you to collaborate on high-profile studies with large, well-known sponsors. The team is part of one of the most prestigious academic research institutes in the world.Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $25.00 - $31.25/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

DescriptionThe Clinical Research Coordinator leads and manages clinical trials in compliance with regulatory standards, working closely with the investigative team, pharmaceutical sponsors, and research participants. This role requires a strong medical background, proficiency in Good Clinical Practices (GCP), FDA regulations, and a commitment to ethical research standards. KEY RESPONSIBILITIES: Duties will include, but are not limited to:• Manage and oversee the execution of clinical trials under the direction of the Principal Investigator and Site Manager.• Conduct patient visits and ensure adherence to study protocols, collecting and processing biological specimens (blood/urine) and performing procedures such as ECGs and vital signs monitoring.• Administer questionnaires, diaries, and other participant materials as per protocol.• Schedule and coordinate research visits, assessments, and procedures, ensuring all requirements are met.• Maintain accurate case report forms, cross-referencing patient medical records for completeness and FDA compliance.• Collect, enter, and manage clinical data while maintaining confidentiality.• Monitor study participants, ensuring adherence to study guidelines and ethical standards.• Manage investigational medications, including receiving, dispensing, and performing drug accountability.• Collaborate with laboratories to process, ship, and ensure review of investigational reports.• Actively participate in recruiting and screening study participants.• Maintain organized records of study materials, ensuring all regulatory documentation is up to date.• Ensure necessary supplies and equipment are available and functional for each study.• Complying with company policies, HIPAA, OSHA regulations, and Standard Operating Procedures (SOPs) to deliver high-quality services.Skillsclinical research, bilingual, bilingual proficiency skills, phlebotomy, phlebotomy certification, phlebotomy certifiedTop Skills Detailsclinical researchAdditional Skills &amp; Qualificationsgood bedside mannerbasic social skills - want patients to feel comfortable and confidentproblem solving skillsEDUCATION REQUIREMENTS:• High School Diploma or GED • Preferred: Bachelor’s or Master’s degree in a related field.EXPERIENCE:• Required: Previous experience conducting clinical trials, including recruitment and compliance with regulatory guidelines.• Preferred: Certification as a Clinical Research Coordinator (CCRC).Experience LevelIntermediate Level<ul><li>This posting is for an existing vacancy.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Fountain Valley, CA.Pay and BenefitsThe pay range for this position is $28.00 - $35.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Fountain Valley,CA.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Coordinator II Job DescriptionThe primary purpose of this role is to conduct clinical research and independently manage both significant aspects of large studies and all aspects of smaller research studies. The position involves working on increasingly complex projects or assignments.Responsibilities<ul><li>Oversee subject recruitment and study enrollment goals.</li><li>Determine effective strategies for promoting and recruiting research participants, as well as retaining participants in long-term clinical trials.</li><li>Oversee data management for research projects by developing and managing systems to organize, collect, report, and monitor data collection.</li><li>Extract, analyze, and interpret data.</li><li>Develop project schedules, targets, measurements, and accountabilities.</li><li>Lead team meetings and prepare or approve minutes.</li><li>Supervise, train, and mentor new staff or students, potentially including hiring and preparing or assisting with performance evaluations.</li><li>Audit operations, including laboratory procedures, to ensure compliance with applicable regulations.</li><li>Provide leadership in identifying and implementing corrective actions and processes.</li><li>Monitor Institutional Review Board submissions and respond to requests and questions.</li><li>Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and resolve study queries.</li><li>Provide leadership in determining, recommending, and implementing improvements to policies and processes and define best practices.</li><li>Develop study budget with staff and principal investigator, identifying standard of care versus study procedures.</li><li>Track patient and study-specific milestones and invoice sponsors according to the study contract.</li><li>Ensure regulatory compliance and regularly inspect study documents to ensure ongoing regulatory compliance.</li><li>Work with the principal investigator to ensure Investigational New Drug applications are submitted to the FDA when applicable, and ensure Institutional Review Board renewals are completed.</li></ul>Essential Skills<ul><li>Minimum of 2-5 years experience as a Clinical Research Coordinator.</li><li>Experience with oncology and complex clinical trials such as Cardio, CAR-T, and Transplant.</li><li>Hands-on experience with interventional sponsored studies, particularly in treatment trials within Phase I-II.</li><li>Experience with patient care during trials.</li><li>Experience coordinating site studies, not in pharma, CRO, or lab research.</li><li>Familiarity with EPIC systems and oncology experience is preferable.</li><li>Ability to conduct chart reviews and pre-screen patients.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience with data coordination and patient visit coordination.</li><li>Experience with EDC (Electronic Data Capture) systems.</li></ul>Work EnvironmentThis position offers a hybrid work environment with 4 days onsite and 1 potential flex day. The role requires 5 days onsite work initially, transitioning to a combination of patient-facing tasks and data management from home after the training period. The opportunity allows you to work with one of the most renowned academic institutions in the US, providing a chance to collaborate closely with a hands-on principal investigator.Job Type &amp; LocationThis is a Contract position based out of Palo Alto, CA.Pay and BenefitsThe pay range for this position is $41.00 - $51.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Palo Alto,CA.Application DeadlineThis position is anticipated to close on Apr 13, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Coordinator II

Clinical Research Coordinator II (Onsite)We are seeking an experienced Clinical Research Coordinator II to support interventional, sponsor‑funded treatment trials (Phase I–II). This is a patient‑facing, onsite role (5 days/week) working closely with investigators and study participants.Key Responsibilities<ul><li>Coordinate patient visits and trial-related care</li><li>Manage study data, documentation, and Epic charting</li><li>Support subject recruitment, screening, and enrollment</li><li>Ensure regulatory compliance and study execution</li><li>Collaborate with investigators, sponsors, and clinical teams</li></ul>Required Qualifications<ul><li>2–5+ years CRC experience (site-based only; no pharma/CRO/lab)</li><li>Experience with interventional sponsored trials (no observational or survey studies)</li><li>Phase I–II treatment trial experience required</li><li>Hands-on patient-facing experience</li><li>Epic EMR experience required</li><li>Background in complex trials (Oncology, Cardio, CAR‑T, Transplant strongly preferred)</li><li>Oncology trial experience</li><li>EDC systems, chart review, and patient pre-screening</li></ul>Job Type &amp; LocationThis is a Contract position based out of Palo Alto, CA.Pay and BenefitsThe pay range for this position is $41.00 - $51.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Palo Alto,CA.Application DeadlineThis position is anticipated to close on Apr 16, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Financial AnalystJob DescriptionWe are seeking a skilled Clinical Research Financial Analyst to manage the financial aspects of clinical trial agreements from initiation through to close out. This role involves reviewing all charges throughout the clinical research trials to ensure financial accuracy and efficiency.Responsibilities<ul><li>Set up and manage clinical trial agreements.</li><li>Oversee the financial life cycle of clinical trials from initiation to close out.</li><li>Review all charges received throughout clinical research trials to ensure accuracy.</li></ul>Essential Skills<ul><li>Experience in clinical trial billing.</li><li>Oncology experience.</li><li>Industry-sponsored trial experience.</li><li>Proficiency in clinical research financial management.</li><li>Data entry skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>3-5 years of relevant experience.</li><li>BS degree preferred.</li></ul>Work EnvironmentThis is a 100% remote position with no restrictions on the states you can work from. The team comprises a Research Finance Manager and three other team members. Our client supports over 200 open clinical trials, primarily in adult and pediatric oncology.Job Type &amp; LocationThis is a Contract to Hire position based out of Providence, RI.Pay and BenefitsThe pay range for this position is $35.00 - $40.86/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Financial Analyst

Job Title: Clinical Research Financial Coordinator (Contract)Job Description:We are seeking a dedicated Financial Coordinator to join our team on a contract basis. This remote position involves managing financial documents and providing support for clinical research studies. The ideal candidate will maintain a sense of urgency and focus on the site’s financial and regulatory needs.Key Responsibilities:<ul><li>Transcribe MCA and Budgets.</li><li>Submit new studies and amendments, partnering with regulatory for document support.</li><li>Check messaging, answer questions, and collaborate with regulatory, leadership to monitor submission status.</li><li>Prepare weekly updates for status reports on study submission/action items and estimated completion times for weekly meetings with the PI.</li><li>Ensure tasks such as email management, coverage analysis submissions to the parent institution, and payment processing and reimbursements are handled promptly and in line with SOPs.</li><li>Research patient visits, process reimbursements, and respond to requests to ensure timely and accurate payments, fostering positive relationships with patients.</li><li>Manage and maintain general email inboxes in accordance with Standard Operating Procedures (SOPs).</li><li>Process patient reimbursement requests and ensure proper filing of emails in designated locations.</li><li>Manage payment confirmations, respond to sponsor requests, and research patient visits in the Electronic Medical Records (EMR) system to facilitate reimbursement.</li></ul>Qualifications:<ul><li>Minimum of three years in a Financial Coordinator role.</li><li>Experience in financial document management and clinical research support.</li><li>Experience in Advarra and WIRB.</li><li>OnCore and Florence experience.</li><li>Strong budgeting experience.</li><li>Strong organizational skills and attention to detail.</li><li>Excellent communication and coordination abilities.</li><li>Ability to work independently and remotely.</li></ul>The following CITI courses are preferred for site files and local IRB portal access:<ul><li>Good Clinical Practice</li><li>Biomedical Investigators and Key Personnel</li><li>Biomedical Responsible Conduct of Research</li><li>Conflicts of Interest</li></ul>Additional Details:Location: Remote - site based in Los Angeles, CADuration: Until February 2027Schedule: 40 hours per week (Monday-Friday) - during normal business hoursStart Date: ASAPJob Type &amp; LocationThis is a Contract position based out of Los Angeles, CA.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Apr 7, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Financial Coordinator

Job Title: Remote Clinical Research Financial Coordinator (Contract)Job DescriptionWe are seeking a highly organized and detail-oriented Clinical Research Financial Coordinator to join our team. The ideal candidate will be responsible for transcribing MCA and Budget into the research site's template, managing study submissions and amendments, and providing financial support to ensure the smooth operation of clinical research studies.Responsibilities<ul><li>Transcribe MCA and Budget prepared into the proper template.</li><li>Work within CS-RAMS, Financial Module, to submit new study and amendments, partnering with regulatory for document support.</li><li>Check CS-RAMS messaging, answer questions, and collaborate with regulatory, leadership, and other stakeholders to monitor submission status.</li><li>Prepare a weekly update for status report on study submission/action items and estimated completion time for weekly meetings with the PI.</li><li>Ensure tasks such as email management, coverage analysis submissions to parent institution, and payment processing and reimbursements are handled promptly and in line with SOPs.</li><li>Research patient visits, process reimbursements, and respond to requests to ensure timely and accurate payments, fostering positive relationships with patients.</li><li>Assist with various financial responsibilities including managing general email inboxes, processing patient reimbursement requests, and ensuring proper filing of emails.</li><li>Manage payment confirmations, respond to sponsor requests, and research patient visits in the Electronic Medical Records (EMR) system to facilitate reimbursement.</li></ul>Essential Skills<ul><li>Clinical trial and clinical research experience</li><li>Data entry skills</li><li>Oncology experience</li><li>Experience with Electronic Data Capture (EDC) systems</li><li>Experience with Electronic Medical Records (EMR) systems</li><li>Experience with Good Clinical Practice</li><li>Experience with Biomedical Investigators and Key Personnel</li><li>Experience with Biomedical Responsible Conduct of Research</li><li>Minimum of 2 years of experience in clinical research financial coordination</li><li>Experience with Advarra and WIRB, and familiarity with Cedars-Sinai local IRB</li><li>Oncore CTMS experience</li><li>Florence experience</li></ul>Additional Skills &amp; Qualifications<ul><li>Ability to work in a fast-paced environment</li><li>Strong attention to detail</li><li>Excellent organizational and communication skills</li><li>Proficiency in Microsoft Office Suite</li></ul>Job Type &amp; LocationThis is a Contract position based out of Eden Prairie, MN.Pay and BenefitsThe pay range for this position is $40.00 - $50.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully remote position.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Nurse﻿Job DescriptionWe are seeking a dedicated Clinical Research Nurse to join our team and play a pivotal role in the safe and effective conduct of clinical trials. You will assist investigators in the preparation and implementation of new clinical trials, screen and enroll participants, and provide comprehensive protocol-related clinical management.Responsibilities<ul><li>Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols using the Study-start up task list.</li><li>Prepare and review study tools, verify approvals, and ensure the scientific and financial readiness of studies prior to activation.</li><li>Conduct one-on-one or group protocol-related nursing education to ensure safe patient care.</li><li>Translate finalized protocol treatment plans into sample orders.</li><li>Work with the clinical research team to ensure timely prescreening of potential subjects for clinical trials.</li><li>Review patient charts and medical history to confirm eligibility and manage informed consent processes.</li><li>Provide back-up support for patient registration with study sponsors and maintain the OnCore® clinical trials database.</li><li>Serve as a critical link between patients and the research team, addressing any challenges and ensuring protocol adherence.</li><li>Coordinate protocol-specified treatments and manage patient reimbursement on clinical trials.</li><li>Deliver high-quality oncology nursing care in coordination with clinical teams and ancillary departments.</li><li>Drive collaboration across medical system staff to ensure timely delivery of services to patients.</li><li>Grade adverse events and ensure accurate documentation and reporting of Serious/Unexpected Adverse Events.</li><li>Ensure compliance with research protocols and assist with monitoring visits and audits.</li><li>Maintain research records for screened and enrolled patients.</li><li>Adhere to all relevant federal, state, and institutional regulations throughout the research process.</li></ul>Essential Skills<ul><li>Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.</li><li>Bachelor’s Degree in Nursing preferred.</li><li>One year of oncology experience required.</li><li>Three to five years of oncology research experience preferred.</li><li>Active Basic Life Support (BLS) certification.</li><li>Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.</li><li>Certification as a Clinical Research Analyst (CRA) or Clinical Research Professional (CCRP) preferred.</li><li>Excellent organizational skills and proficiency in computer applications.</li><li>Strong communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Detail-oriented with excellent organizational skills.</li><li>Proficient in computer applications such as Word and Excel.</li><li>Resourceful and able to maximize resources effectively.</li><li>Equivalent education, experience, and/or training may be substituted for the degree requirement.</li></ul>Work EnvironmentJoin a team that is a leader in scientific discovery and transdisciplinary engagement aimed at improving cancer outcomes. We conduct innovative research, offer cutting-edge patient-centered care, and develop new therapies to decrease cancer incidence and mortality. The team is located across multiple sites, including Newark, and operates 300 active trials with a goal of enrolling 2,500 subjects per year across all phases, including adult and pediatric trials.Job Type &amp; LocationThis is a Contract to Hire position based out of Livingston, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Livingston,NJ.Application DeadlineThis position is anticipated to close on Apr 9, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Nurse

<h2>Clinical Research Nurse</h2>Key Responsibilities: <ul><li>Recruit, screen, and enroll participants into clinical trials.</li><li>Explain the informed consent process to potential study subjects and ensure proper documentation.</li><li>Document and report adverse events in accordance with study and regulatory guidelines.</li><li>Collect, organize, and maintain study-related materials, including:<ul><li>Study documents</li><li>Protocols</li><li>Regulatory files</li><li>Informed consent forms</li><li>Case report forms (CRFs)</li><li>Source documents</li></ul></li><li>Prepare and submit applications to the Institutional Review Board (IRB) and ensure compliance with human subject protection regulations.</li><li>Conduct chart reviews, maintain accurate documentation, and support data entry in Electronic Data Capture (EDC) systems.</li><li>Communicate effectively with patients, study sponsors, investigators, and internal teams</li></ul>Qualifications: <ul><li>BA/BS preferred</li><li>2+ years of clinical research experience required</li><li>Experience in in-hospital clinical research settings</li><li>Experience with adverse event reporting</li><li>Familiarity with IRB processes and human research protection regulations</li><li>Ability to work collaboratively in a fast‑paced research environment</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $40.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research Nurse﻿Job DescriptionAs a Clinical Research Nurse, you will play a pivotal role in coordinating and implementing inpatient and outpatient cardiovascular clinical research studies. Your efforts will directly impact the future of medicine, patients, and their families. This position involves coordinating all procedures, tests, and follow-up visits according to protocol for enrolled research subjects, collecting study data, complying with regulatory requirements, and monitoring and reporting adverse events.Responsibilities<ul><li>Coordinate and implement inpatient and outpatient cardiovascular clinical research studies.</li><li>Coordinate all procedures, tests, and follow-up visits according to the protocol for enrolled research subjects.</li><li>Collect study data and comply with regulatory requirements.</li><li>Monitor and report adverse events for study subjects.</li><li>Provide education to research subjects and staff regarding the investigational study.</li><li>Promote patient safety for all research-related activities.</li><li>Collaborate with physician investigators and a multi-disciplinary team.</li><li>Utilize strong computer-based skills for reporting purposes.</li></ul>Essential Skills<ul><li>1+ years of nursing experience</li><li>Clinical Trials/Clinical Research experience preferred.</li><li>Excellent organizational skills.</li><li>Experience with Microsoft Office.</li><li>Experience with electronic medical records programs preferred.</li><li>Current Pennsylvania RN license.</li></ul>Additional Skills &amp; Qualifications<ul><li>Graduation from an accredited school of professional nursing required.</li><li>BSN preferred.</li><li>Hospital credentialing as required.</li><li>Successful completion of CITI Program &amp; CPR certification.</li><li>IATA &amp; ACRP research certification encouraged.</li></ul>Work EnvironmentThis role requires working 5 days on site at Wynnewood, with occasional travel to Bryn Mawr as needed. The schedule will be communicated weeks in advance.Job Type &amp; LocationThis is a Contract to Hire position based out of Wynnewood, PA.Pay and BenefitsThe pay range for this position is $42.00 - $45.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Wynnewood,PA.Application DeadlineThis position is anticipated to close on Apr 6, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Research Nurse Clinician (RNC) is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. The RNC assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and provides protocol-related clinical management to those participants. This role serves as a resource for faculty and staff on available protocols and general research topics such as FDA, IRB, and GCP regulations.Responsibilities<ul><li>Collaborate with the Protocol Activation office to initiate and activate all new clinical trial protocols utilizing a study start-up task list.</li><li>Prepare and review study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.</li><li>Verify Scientific Review Board, Institutional Review Board, data collection plans, and finance/contract approvals prior to study activation.</li><li>Review protocols and collect multidisciplinary logistical, educational, and financial feedback to identify and resolve potential obstacles.</li><li>Perform protocol-related nursing education for other disciplines to ensure safe and effective care of enrolled patients.</li><li>Translate protocol treatment plans into sample orders.</li><li>Collaborate with the clinical research team for timely prescreening of potential subjects for clinical trials.</li><li>Review patient charts and medical history to confirm protocol eligibility and obtain necessary source documents.</li><li>Ensure informed consent is obtained and documented in accordance with IRB, GCP, and institutional policies.</li><li>Register consented research patients with study sponsors and input information into the OnCore® clinical trials database.</li><li>Serve as an essential link between patients and research team members, identifying and addressing any challenges.</li><li>Ensure protocol-specific orders are executed accurately, coordinating protocol-specified treatments between disciplines.</li><li>Manage patient reimbursements and deliver high-quality oncology nursing care in coordination with clinical teams.</li><li>Facilitate collaboration with academic medical system staff to ensure coordinated and timely delivery of services.</li><li>Grade adverse events using NCI common toxicity criteria and complete Serious/Unexpected Adverse Event forms.</li><li>Assist with monitoring visits and audits, providing responses to sponsor queries.</li><li>Maintain research records and ensure compliance with all relevant regulations and standards.</li></ul>Essential Skills<ul><li>Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.</li><li>Bachelor’s Degree in Nursing preferred.</li><li>One year of oncology experience required.</li><li>Three to five years of oncology research experience preferred.</li><li>Active Basic Life Support (BLS) certification.</li><li>Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.</li><li>Detail-oriented with excellent organizational skills.</li><li>Proficiency in computer applications such as Word and Excel.</li><li>Excellent communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred.</li><li>Experience in clinical research coordination, patient screening, and study coordination.</li><li>Comfortable communicating with patients.</li></ul>Work EnvironmentThe work environment is dynamic and focused on scientific discovery, patient care, and education. The organization is a leader in conducting innovative basic, clinical, and population research. The facility has a vision to improve outcomes for cancer patients through patient-centered care and transdisciplinary engagement. The team comprises clinical operations, QA, informatics, finance, and education, with a significant number of active trials and subjects enrolled annually. The work involves collaboration across multiple sites and disciplines, contributing to a robust research infrastructure.Job Type &amp; LocationThis is a Contract to Hire position based out of New Brunswick, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in New Brunswick,NJ.Application DeadlineThis position is anticipated to close on Mar 31, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Clinical Research Nurse Coordinator

Job Title: Clinical Research Nurse Job DescriptionThe primary role of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This position involves collaborating with various departments to initiate and activate new clinical trial protocols, providing protocol-related clinical management to study participants, and serving as a resource for other staff on research topics such as FDA, IRB, and GCP regulations.Responsibilities<ul><li>Collaborate with the Protocol Activation office to initiate and activate all new clinical trial protocols using the study start-up task list.</li><li>Prepare and review study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.</li><li>Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals prior to study activation.</li><li>Review protocols and collect multidisciplinary logistical, educational, and financial feedback to identify potential obstacles to safe, effective study conduct.</li><li>Perform protocol-related nursing education to other disciplines to facilitate safe, effective care of enrolled patients.</li><li>Translate finalized protocol treatment plans, study calendars, and clinical trials billing grids into sample orders.</li><li>Collaborate with the clinical research team to ensure timely prescreening of potential subjects and active cancer patients for clinical trials.</li><li>Review patient charts and medical history to confirm protocol eligibility and obtain source documents as needed.</li><li>Ensure informed consent is obtained, signed, placed in the medical record, and a copy provided to the patient.</li><li>Provide back-up support to register consented research patients with study sponsors and input data into the clinical trials database.</li><li>Coordinate continuity of protocol-specified procedures and treatments for study patients between disciplines/sites of care.</li><li>Manage high-quality, compassionate hands-on oncology nursing care and coordinate with clinical teams, investigators, and ancillary departments.</li><li>Ensure protocol-specific orders are entered and executed accurately, including scheduling and completion of tests and appointments.</li><li>Drive collaboration with integrated medical system staff to ensure coordinated and timely delivery of services to patients.</li><li>Grade adverse events using protocol-referenced criteria and complete Serious/Unexpected Adverse Event (SAE) forms as required.</li><li>Assist with monitoring visits, audits, and database queries as needed.</li><li>Maintain research records for screened and enrolled patients and ensure compliance with institutional, state, and federal regulations.</li></ul>Essential Skills<ul><li>Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.</li><li>Bachelor's Degree in Nursing preferred.</li><li>One year of oncology experience required.</li><li>Three to five years of oncology research experience preferred.</li><li>Maintains active Basic Life Support (BLS) certification.</li><li>Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.</li><li>Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred.</li></ul>Additional Skills &amp; Qualifications<ul><li>Detail-oriented with excellent organizational skills.</li><li>Proficient in computer applications (Word, Excel, etc.).</li><li>Excellent communication and interpersonal skills.</li><li>Ability to maximize resources and be resourceful.</li><li>Equivalent education, experience, and/or training may be substituted for the degree requirement.</li></ul>Work EnvironmentOur vision is to be a leader in scientific discovery, transdisciplinary engagement, translation, patient care, and education to improve outcomes for cancer patients. We conduct innovative research and patient-centered care, facilitating rapid translation of laboratory-based discoveries into human studies. The work environment includes 40 full-time equivalents in clinical operations, disease-specific groups, quality assurance, informatics, education, and finance. We have 100 full-time equivalents and enroll 5,000 subjects per year across multiple sites.Job Type &amp; LocationThis is a Contract to Hire position based out of New Brunswick, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $60.00/hr.Eligibility requirements apply to some benefits and may depend on your job
 classification and length of employment. Benefits are subject to change and may be
 subject to specific elections, plan, or program terms. If eligible, the benefits
 available for this temporary role may include the following:

 • Medical, dental &amp; vision
 • Critical Illness, Accident, and Hospital
 • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
 • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents)
 • Short and long-term disability
 • Health Spending Account (HSA)
 • Transportation benefits
 • Employee Assistance Program
 • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in New Brunswick,NJ.Application DeadlineThis position is anticipated to close on Apr 7, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Cardiovascular Research NursePosition: Cardiovascular Research NurseSchedule: Full-time | Flexible hours based on study needs (typically M–F, between 7:00–8:00 AM start, 8‑hour shifts). Occasional weekend work mayoccur but is rare.Location: Orlando, FL About the RoleWe are seeking a highly skilled and motivated Cardiovascular Research Nurse to join our research team. The ideal candidate will be responsible for delivering safe, high-quality patient care while supporting clinical research protocols—primarily Phase 3 trials—with a current trial load of approximately 8–10 studies.This role requires strong clinical assessment abilities, adherence to regulatory standards, and the capacity to work both independently and collaboratively in a fast‑paced clinical research environment.Key Responsibilities<ul><li>Provide safe, compassionate care that upholds the dignity and respect of all research participants.</li><li>Maintain clinical competencies including: <ul></ul></li><li class="ql-indent-1">Physical assessments</li><li class="ql-indent-1">Phlebotomy</li><li class="ql-indent-1">IV insertion</li><li>Perform clinical tasks within the nursing scope of practice to support physicians, ARNPs, and Clinical Research Nurses during minor procedures and study‑related requirements.</li><li>Administer investigational medications (currently all oral agents) in alignment with AdventHealth policies and clinical research standards.</li><li>Apply Universal Precautions and adhere to HIPAA regulations at all times.</li><li>Work efficiently and independently while managing multiple tasks simultaneously in a dynamic clinical and research setting.</li><li>Support the execution of Phase 3 cardiovascular clinical trials; role involves active, hands‑on study involvement.</li><li>Ensure accurate documentation and follow all Good Clinical Practice (GCP) guidelines.</li></ul>Qualifications Candidates with 5+ years of RN experience in any of the following areas will be considered, even without prior research experience: <ul><ul></ul><li>Cardiovascular</li><li>Critical Care</li><li>Transplant</li></ul>Previous clinical research experience is a strong plus but not required for candidates with robust specialty backgrounds.Associate’s Degree in Nursing (ASN) required; Bachelor of Science in Nursing (BSN) preferredActive Florida RN license Advanced Cardiac Life Support(ACLS) AND Basic Life Support (BLS) Job Type &amp; LocationThis is a Permanent position based out of Orlando, FL.Pay and BenefitsThe pay range for this position is $83200.00 - $100000.00/yr.All the benefits and perks you need for you and your family:

Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance

Paid Time Off from Day One

403-B Retirement Plan

4 Weeks 100% Paid Parental Leave

Career Development

Whole Person Well-being Resources

Mental Health Resources and Support

Pet BenefitsWorkplace TypeThis is a fully onsite position in Orlando,FL.Application DeadlineThis position is anticipated to close on Apr 10, 2026.<h2>Diversity, Equity &amp; Inclusion</h2> At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&amp;I is embedded into our culture through: <ul><li>Hiring diverse talent</li> <li>Maintaining an inclusive environment through persistent self-reflection</li> <li>Building a culture of care, engagement, and recognition with clear outcomes</li> <li>Ensuring growth opportunities for our people</li> </ul> Actalent is an equal opportunity employer. <h2>About Actalent</h2> Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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