<h2 style="text-align:center;">Clinical Laboratory Technician</h2>Cell &amp; Molecular Immunology Group | Entry-level | $25/hrJob DescriptionThe Clinical Laboratory Technician performs analyses on blood, tissue, and body fluids to assist healthcare providers in the diagnosis, prognosis, and treatment of patients. The role involves participating in operational support activities necessary to maintain and optimize testing capabilities. Testing is conducted in specialized laboratories using highly skilled manual techniques or automated testing with sophisticated instrumentation.Responsibilities<ul><li>Operate and maintain laboratory instruments.</li><li>Troubleshoot assays and evaluate tests for accuracy.</li><li>Assist with interpreting results.</li><li>Engage in operational support activities to optimize testing.</li><li>Work with multiple computer systems for retrieving information and reporting results.</li><li>Possibly assist with specimen collection.</li><li>Isolate and manipulate PBMCs from patient blood specimens in a BioSafety Cabinet.</li><li>Use manual pipettes and demonstrate manual dexterity for laboratory techniques.</li><li>Freeze, thaw, and plate cells for clinical assays.</li><li>Learn and apply aseptic techniques, if not already experienced.</li><li>Learn and use several software programs required for clinical lab technologists.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in chemistry or a human biological science is required (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Neuroscience).</li></ul>Work EnvironmentThe work schedule is from 7:30 AM to 4 PM, Monday to Friday, with no weekend shifts. Job Type &amp; LocationThis is a Contract to Hire position based out of Rochester, MN.Pay and BenefitsThe pay range for this position is $25.00 - $25.00/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 Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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Clinical Laboratory Technician

<h2>Clinical Lab Specialist</h2>﻿Job DescriptionApply advanced knowledge of clinical lab testing to perform independent work and train others. Adapt and modify lab methods to solve complex problems and validate new tests. Handle sample processing, including integrity checks, data verification, and bacterial culturing.Responsibilities<ul><li>Perform independent work and train others in the laboratory setting.</li><li>Adapt and modify laboratory methods to solve complex problems and validate new tests.</li><li>Handle sample processing, including integrity checks, data verification, and bacterial culturing.</li><li>Send samples to CDC and regional labs for specialized testing.</li><li>Conduct small animal necropsies and prepare brain samples for rabies testing.</li><li>Operate, maintain, and troubleshoot a wide range of laboratory instruments, such as MALDI-ToF and Illumina MiSeq.</li><li>Perform whole genome sequencing and analyze data using bioinformatics tools like Bionumerics and BugSeq.</li><li>Document patient and testing information in accordance with CLIA regulations, and write SOPs and validation studies.</li><li>Promote and troubleshoot quality control, initiate corrective actions, and support QA/QI efforts.</li><li>Monitor reagent inventory and expiration, and recommend equipment upgrades as needed.</li><li>Oversee testing operations for microbiology, bioterrorism response, and quality assurance programs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biology, microbiology, clinical lab science, or a related field—or equivalent education and experience.</li><li>Minimum of 4 years’ experience performing high-complexity clinical testing using traditional and molecular methods.</li><li>Experience in bacteriology and microbiology within a clinical laboratory setting.</li><li>Prior experience in both public health and clinical testing laboratories.</li><li>Certification as MLS or MLT by ASCP or AMT is highly desirable.</li><li>Experience with QA procedures, lab safety protocols, and Windows-based systems.</li><li>Familiarity with high-volume, fast-paced clinical lab environments.</li><li>Proven ability to report results and maintain quality standards in diagnostic testing.Lab</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Iowa City, IA.Pay and BenefitsThe pay range for this position is $26.00 - $28.00/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 Iowa City,IA.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Microbiology Technician

<h2>Clinical Lab Specialist</h2>﻿Job DescriptionApply advanced knowledge of clinical lab testing to perform independent work and train others. Adapt and modify lab methods to solve complex problems and validate new tests. Handle sample processing, including integrity checks, data verification, and bacterial culturing.Responsibilities<ul><li>Perform independent work and train others in the laboratory setting.</li><li>Adapt and modify laboratory methods to solve complex problems and validate new tests.</li><li>Handle sample processing, including integrity checks, data verification, and bacterial culturing.</li><li>Send samples to CDC and regional labs for specialized testing.</li><li>Conduct small animal necropsies and prepare brain samples for rabies testing.</li><li>Operate, maintain, and troubleshoot a wide range of laboratory instruments, such as MALDI-ToF and Illumina MiSeq.</li><li>Perform whole genome sequencing and analyze data using bioinformatics tools like Bionumerics and BugSeq.</li><li>Document patient and testing information in accordance with CLIA regulations, and write SOPs and validation studies.</li><li>Promote and troubleshoot quality control, initiate corrective actions, and support QA/QI efforts.</li><li>Monitor reagent inventory and expiration, and recommend equipment upgrades as needed.</li><li>Oversee testing operations for microbiology, bioterrorism response, and quality assurance programs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biology, microbiology, clinical lab science, or a related field—or equivalent education and experience.</li><li>Minimum of 4 years’ experience performing high-complexity clinical testing using traditional and molecular methods.</li><li>Experience in bacteriology and microbiology within a clinical laboratory setting.</li><li>Prior experience in both public health and clinical testing laboratories.</li><li>Certification as MLS or MLT by ASCP or AMT is highly desirable.</li><li>Experience with QA procedures, lab safety protocols, and Windows-based systems.</li><li>Familiarity with high-volume, fast-paced clinical lab environments.</li><li>Proven ability to report results and maintain quality standards in diagnostic testing.Lab</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Iowa City, IA.Pay and BenefitsThe pay range for this position is $26.00 - $28.00/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 Iowa City,IA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Clinical Lab Specialist</h2>﻿Job DescriptionApply advanced knowledge of clinical lab testing to perform independent work and train others. Adapt and modify lab methods to solve complex problems and validate new tests. Handle sample processing, including integrity checks, data verification, and bacterial culturing.Responsibilities<ul><li>Perform independent work and train others in the laboratory setting.</li><li>Adapt and modify laboratory methods to solve complex problems and validate new tests.</li><li>Handle sample processing, including integrity checks, data verification, and bacterial culturing.</li><li>Send samples to CDC and regional labs for specialized testing.</li><li>Conduct small animal necropsies and prepare brain samples for rabies testing.</li><li>Operate, maintain, and troubleshoot a wide range of laboratory instruments, such as MALDI-ToF and Illumina MiSeq.</li><li>Perform whole genome sequencing and analyze data using bioinformatics tools like Bionumerics and BugSeq.</li><li>Document patient and testing information in accordance with CLIA regulations, and write SOPs and validation studies.</li><li>Promote and troubleshoot quality control, initiate corrective actions, and support QA/QI efforts.</li><li>Monitor reagent inventory and expiration, and recommend equipment upgrades as needed.</li><li>Oversee testing operations for microbiology, bioterrorism response, and quality assurance programs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biology, microbiology, clinical lab science, or a related field—or equivalent education and experience.</li><li>Minimum of 4 years’ experience performing high-complexity clinical testing using traditional and molecular methods.</li><li>Experience in bacteriology and microbiology within a clinical laboratory setting.</li><li>Prior experience in both public health and clinical testing laboratories.</li><li>Certification as MLS or MLT by ASCP or AMT is highly desirable.</li><li>Experience with QA procedures, lab safety protocols, and Windows-based systems.</li><li>Familiarity with high-volume, fast-paced clinical lab environments.</li><li>Proven ability to report results and maintain quality standards in diagnostic testing.Lab</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Iowa City, IA.Pay and BenefitsThe pay range for this position is $26.00 - $28.00/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 Iowa City,IA.Application DeadlineThis position is anticipated to close on Mar 2, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Clinical Lab Specialist</h2>﻿Job DescriptionApply advanced knowledge of clinical lab testing to perform independent work and train others. Adapt and modify lab methods to solve complex problems and validate new tests. Handle sample processing, including integrity checks, data verification, and bacterial culturing.Responsibilities<ul><li>Perform independent work and train others in the laboratory setting.</li><li>Adapt and modify laboratory methods to solve complex problems and validate new tests.</li><li>Handle sample processing, including integrity checks, data verification, and bacterial culturing.</li><li>Send samples to CDC and regional labs for specialized testing.</li><li>Conduct small animal necropsies and prepare brain samples for rabies testing.</li><li>Operate, maintain, and troubleshoot a wide range of laboratory instruments, such as MALDI-ToF and Illumina MiSeq.</li><li>Perform whole genome sequencing and analyze data using bioinformatics tools like Bionumerics and BugSeq.</li><li>Document patient and testing information in accordance with CLIA regulations, and write SOPs and validation studies.</li><li>Promote and troubleshoot quality control, initiate corrective actions, and support QA/QI efforts.</li><li>Monitor reagent inventory and expiration, and recommend equipment upgrades as needed.</li><li>Oversee testing operations for microbiology, bioterrorism response, and quality assurance programs.</li></ul>Essential Skills<ul><li>Bachelor’s degree in biology, microbiology, clinical lab science, or a related field—or equivalent education and experience.</li><li>Minimum of 4 years’ experience performing high-complexity clinical testing using traditional and molecular methods.</li><li>Experience in bacteriology and microbiology within a clinical laboratory setting.</li><li>Prior experience in both public health and clinical testing laboratories.</li><li>Certification as MLS or MLT by ASCP or AMT is highly desirable.</li><li>Experience with QA procedures, lab safety protocols, and Windows-based systems.</li><li>Familiarity with high-volume, fast-paced clinical lab environments.</li><li>Proven ability to report results and maintain quality standards in diagnostic testing.Lab</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Iowa City, IA.Pay and BenefitsThe pay range for this position is $26.00 - $28.00/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 Iowa City,IA.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: REMS Clinical Nurse EducatorJob DescriptionThe Risk Evaluation and Mitigation Strategy (REMS) Clinical Nurse Educator plays a pivotal role in delivering high-quality patient care and counseling to those enrolled in the Medication Therapy Program. The ideal candidate is passionate, possesses excellent communication skills, attention to detail, problem-solving capabilities, and is self-motivated to support team members in achieving the mission of providing exceptional patient care.Responsibilities<ul><li>Counsel and educate patients on REMS FDA-mandated medications, including reading statements to patients verbatim.</li><li>Ensure patients and caregivers are educated about their current therapy, medication adherence, and handle medication refill deliveries and copay collections as applicable.</li><li>Maintain adherence to contracted and accrediting regulations as specified by drug specifications.</li><li>Complete thorough and accurate documentation following good documentation practices and compliance with industry standards and regulations.</li><li>Discuss potential or current side effects with patients to educate them about treatment alternatives and facilitate ongoing therapy adherence.</li><li>Identify and report adverse events and product complaints to the manufacturer, FDA, and other governing authorities.</li><li>Verify specialty drugs and educate patients; act as a conduit between providers and patients to support therapeutic longevity.</li><li>Maintain patient demographic records, medical history, and records according to federal HIPAA standards.</li><li>Collaborate with Pharmacy Support teams to ensure timely and accurate delivery of specialty drugs.</li></ul>Essential Skills<ul><li>Registered Nurse with a current unrestricted compact state license or primary NC licensure.</li><li>Associates, Bachelor, or higher degree in Nursing or accredited nursing diploma.</li><li>Ability to obtain licensing in all states and United States territories serviced within 3 months of employment.</li><li>5 or more years of nursing experience, with at least 1 year in inpatient or outpatient care preferred.</li><li>Proficiency in computer skills, including email, word processing, spreadsheet, and web-based programs.</li><li>Effective communication skills both orally and in writing, with experience in motivational interviewing preferred.</li><li>Ability to read, analyze, and interpret practice standards, professional journals, and technical procedures.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology nursing is advantageous.</li><li>Skills in risk evaluation and mitigation strategies are desirable.</li><li>Proficiency in computer data entry and phone etiquette.</li></ul>Work EnvironmentAfter the training period, the role will involve working two days in the office and three days from home, contingent on meeting metrics. The team works remotely, with working hours from Monday to Friday, 9 am to 6 pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Cary, NC.Pay and BenefitsThe pay range for this position is $40.00 - $40.00/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 Cary,NC.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Nurse Educator

Job Title: REMS Clinical Nurse EducatorJob DescriptionThe Risk Evaluation and Mitigation Strategy (REMS) Clinical Nurse Educator plays a pivotal role in delivering high-quality patient care and counseling to those enrolled in the Medication Therapy Program. The ideal candidate is passionate, possesses excellent communication skills, attention to detail, problem-solving capabilities, and is self-motivated to support team members in achieving the mission of providing exceptional patient care.Responsibilities<ul><li>Counsel and educate patients on REMS FDA-mandated medications, including reading statements to patients verbatim.</li><li>Ensure patients and caregivers are educated about their current therapy, medication adherence, and handle medication refill deliveries and copay collections as applicable.</li><li>Maintain adherence to contracted and accrediting regulations as specified by drug specifications.</li><li>Complete thorough and accurate documentation following good documentation practices and compliance with industry standards and regulations.</li><li>Discuss potential or current side effects with patients to educate them about treatment alternatives and facilitate ongoing therapy adherence.</li><li>Identify and report adverse events and product complaints to the manufacturer, FDA, and other governing authorities.</li><li>Verify specialty drugs and educate patients; act as a conduit between providers and patients to support therapeutic longevity.</li><li>Maintain patient demographic records, medical history, and records according to federal HIPAA standards.</li><li>Collaborate with Pharmacy Support teams to ensure timely and accurate delivery of specialty drugs.</li></ul>Essential Skills<ul><li>Registered Nurse with a current unrestricted compact state license or primary NC licensure.</li><li>Associates, Bachelor, or higher degree in Nursing or accredited nursing diploma.</li><li>Ability to obtain licensing in all states and United States territories serviced within 3 months of employment.</li><li>5 or more years of nursing experience, with at least 1 year in inpatient or outpatient care preferred.</li><li>Proficiency in computer skills, including email, word processing, spreadsheet, and web-based programs.</li><li>Effective communication skills both orally and in writing, with experience in motivational interviewing preferred.</li><li>Ability to read, analyze, and interpret practice standards, professional journals, and technical procedures.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology nursing is advantageous.</li><li>Skills in risk evaluation and mitigation strategies are desirable.</li><li>Proficiency in computer data entry and phone etiquette.</li></ul>Work EnvironmentAfter the training period, the role will involve working two days in the office and three days from home, contingent on meeting metrics. The team works remotely, with working hours from Monday to Friday, 9 am to 6 pm.Job Type &amp; LocationThis is a Contract to Hire position based out of Cary, NC.Pay and BenefitsThe pay range for this position is $40.00 - $40.00/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 Cary,NC.Application DeadlineThis position is anticipated to close on Feb 23, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical PharmacistJob DescriptionThe Clinical Pharmacy Specialist plays a vital role in contributing to the prevention and cure of cancer by providing safe, evidence-based, cost-effective, and patient-centered medication management. As an integral member of the Malignant Hematology interdisciplinary team, the Clinical Specialist offers clinical pharmacy support to healthcare professionals and ensures optimal patient outcomes by recommending, designing, implementing, monitoring, and modifying pharmaceutical care plans.Responsibilities<ul><li>Provide oversight for the safe and appropriate use of medication prescribing, dispensing, administering, and monitoring.</li><li>Deliver clinical pharmaceutical care to optimize drug therapy for cancer patients through recommendation, implementation, monitoring, and modification of individualized treatment plans in collaboration with the healthcare team.</li><li>Perform medication order review, clarification, and verification, assessing for completeness and appropriateness.</li><li>Supervise accurate hazardous and non-hazardous drug preparation and distribution per policies and procedures.</li><li>Process and double-check chemotherapy orders as necessary.</li><li>Develop, interpret, and provide medication-related information and education for pharmacists, providers, nurses, and other healthcare personnel.</li><li>Coordinate and provide medication therapy education and counseling to patients and caregivers.</li><li>Precept pharmacy students, residents, and others in training.</li><li>Participate in clinical research and projects.</li><li>Provide leadership for developing, implementing, and maintaining medication-related guidelines, policies, and standards.</li><li>Manage the medication use process to improve workflow, quality, and safety for patients and staff.</li><li>Oversee the cost-effective use of medications to ensure appropriate utilization of resources and reduce financial risk.</li></ul>Essential Skills<ul><li>Doctor of Pharmacy Degree</li><li>Board of Pharmacy Specialties (BPS) certification</li><li>Experience in medication management, oncology, and malignant hematology</li><li>Ability to develop and implement pharmaceutical care plans</li><li>Knowledge of medication safety, formulary management, and policy development</li></ul>Additional Skills &amp; Qualifications<ul><li>PGY-2 Residency in Hematology/Oncology</li><li>Experience in chemotherapy order processing</li><li>Experience in clinical research</li><li>Skill in education of patients, family members, healthcare providers, and pharmacy students and residents</li></ul>Work EnvironmentThe work environment offers a supportive and collaborative atmosphere, emphasizing teamwork and patient-centered care. The schedule includes 7-on/7-off options and hybrid flexibility. Employees can expect a clean and safe environment, with opportunities for professional growth and development. A strong emphasis is placed on maintaining work-life balance, and comprehensive benefits are provided, including health, dental, and vision plans, retirement plans, and wellness programs.Job Type &amp; LocationThis is a Permanent position based out of Tampa, FL.Pay and BenefitsThe pay range for this position is $120000.00 - $180000.00/yr.health/dental/vision insurance, retirement (403B) with a competitive match, generous PTO/vacation/sick days, paid holidays, life/disability insurance, wellness programs (gym), and professional developmentWorkplace TypeThis is a hybrid position in Tampa,FL.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Pharmacist

Job Title: Clinical Project ManagerJob DescriptionWe are seeking a dedicated Clinical Project Manager with extensive experience in clinical research to lead and manage our oncology studies. The candidate will play a pivotal role in overseeing study start-ups and managing clinical trials, particularly in the field of oncology.Responsibilities<ul><li>Lead and manage clinical research studies, with a strong focus on oncology projects.</li><li>Oversee study start-ups and ensure timely patient enrollment and consent processes.</li><li>Coordinate with clinical research teams, including Clinical Research Coordinators and Nurses, to ensure smooth operation of clinical trials.</li><li>Manage vendor relationships and ensure compliance with clinical trial protocols.</li><li>Provide oversight and guidance to staff, ensuring effective line management and project management practices.</li></ul>Essential Skills<ul><li>Minimum of 4 years of experience in clinical research.</li><li>Proven experience in running clinical studies.</li><li>Strong background in oncology research.</li><li>Expertise in patient enrollment, informed consent processes, and clinical trial management.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a relevant field is required; a Master's degree is preferred.</li><li>Experience in staff oversight and line management.</li><li>Proficiency in vendor and portfolio management.</li></ul>Work EnvironmentThe work environment is a dynamic combination of office and hospital/outpatient surgery settings. You will be part of a fast-paced and high-volume workload environment, managing 27 active studies with a team of 8 staff members. The team consists of 4 Clinical Research Coordinators, 3 Clinical Research Nurses, and 1 Lead Clinical Research Nurse/Program Manager. You will have the opportunity to work with state-of-the-art equipment and engage in high-profile studies with renowned sponsors.Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $32.00 - $36.00/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 Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Project Manager

<h2>Job Title: Clinical Research Associate</h2>Job DescriptionThe Clinical Research Associate will focus primarily on data management for clinical trials and act as a backup for regulatory associates. Initially, the role involves working with Registry studies, including pre-screening, recruiting, consenting, and following up with participants. This will occupy approximately 40% of the time, with the remainder dedicated to data entry, data management, and assisting the Research Nurse during patient visits.Responsibilities<ul><li>Manage data for clinical trials and serve as a backup for regulatory associates.</li><li>Work with Registry studies, including pre-screening, recruiting, consenting, and follow-up activities.</li><li>Perform data entry and data management tasks.</li><li>Assist the Research Nurse with patient visits.</li></ul>Required Skills &amp; Experience<ul><li>Minimum of 1 year of clinical research experience</li><li>Understanding of clinical trials terminology</li><li>Proficiency in EDC systems, with the ability to learn various systems</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology is ideal</li><li>Willingness to undergo oncology training</li></ul>Job Type &amp; LocationThis is a Contract position based out of Grosse Pointe Woods, MI.Pay and BenefitsThe pay range for this position is $20.00 - $31.00/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 Grosse Pointe Woods,MI.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Associate

Job Title: Clinical Research CoordinatorJob DescriptionThe Research Coordinator will assist with implementing research study tasks. This involves recruitment, data collection, data management, and reporting of results, supporting a seamless research process.Responsibilities<ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including eligibility screening.</li><li>Perform follow-up with study participants via telephone, email, and mail.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul>Essential Skills<ul><li>High school diploma or General Education Development (GED).</li><li>6+ months of clinical research experience.</li><li>Experience in the medical field, including phlebotomy and vaccines.</li></ul>Additional Skills &amp; Qualifications<ul><li>Tech savvy.</li><li>Interest in growing in clinical research.</li><li>Proficiency in data entry.</li></ul>Job Type &amp; LocationThis is a Contract position based out of Winston-Salem, NC.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 Winston-Salem,NC.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator to oversee and manage diagnostic breast imaging studies. The role involves preparing and processing all Institutional Review Board (IRB) documents and coordinating essential documentation required by sponsors or CROs. This position ensures the accurate reporting of adverse events in compliance with relevant regulations and protocols.Responsibilities<ul><li>Coordinate diagnostic breast imaging studies.</li><li>Prepare and process initial submissions, amendments, and continuing reviews through the Institutional Review Board (IRB) and other regulatory bodies.</li><li>Organize and maintain all documentation required by sponsors or CROs, including case report forms, source documentation, study and regulatory binders, and subject binders.</li><li>Ensure proper reporting of serious and non-serious adverse events to the Sponsor and all applicable institutional or study-related committees and personnel, such as the IRB, DSMC, DSMB/Medical Monitor.</li></ul>Essential Skills<ul><li>Bachelor of Science degree.</li><li>2 to 3 years of clinical research experience or an equivalent combination of education and experience.</li><li>Prior experience with clinical trials required.</li><li>Proficiency in clinical research, data management, patient recruitment, and enrollment.</li><li>Experience with chart review, data entry, and screening.</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong organizational and communication skills.</li><li>Ability to work collaboratively in a team environment.</li></ul>Work EnvironmentThis position offers a hybrid schedule, with on-site work required. Our mission is to provide advanced breast imaging technology for precise detection and diagnosis of breast diseases. The work environment supports high-quality interventional breast procedures, including stereotactic, ultrasound-guided, and MRI-guided biopsies.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 - $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 hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research CoordinatorJob DescriptionThe Clinical Research Coordinator will oversee study coordination, including study start-up, patient recruitment, and providing backup support as needed. The role involves collaborating closely with Principal Investigators to ensure effective trial management and communication.Responsibilities<ul><li>Serve as the primary contact to ensure appropriate communications, trial management, and meeting of timelines.</li><li>Coordinate the operational aspects of new and ongoing clinical trials at the site.</li><li>Work under the supervision of the Principal Investigator(s), exercising excellent clinical judgment in patient monitoring and care.</li><li>Maintain daily contact with the Principal Investigator(s) for recruitment activities, study start-up, and general communication.</li><li>Ensure protocol execution and proper delegation and training of all staff working on protocols.</li><li>Conduct patient recruitment and pre-screening.</li><li>Maintain and submit IRB communications and regulatory documents.</li><li>Communicate timely with internal teams, investigators, review boards, and study subjects.</li><li>Prepare study materials as requested by the Principal Investigator, such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>Patient recruitment</li><li>Clinical trial management</li><li>Clinical research</li><li>Good Clinical Practice (GCP)</li><li>Oncology</li><li>Phlebotomy</li></ul>Additional Skills &amp; Qualifications<ul><li>At least a High School Diploma is required.</li><li>3+ years of prior Clinical Research Coordinator experience is required.</li><li>Oncology experience is essential.</li><li>Strong management and organizational skills, with an understanding of medical procedures.</li><li>Exceptional interpersonal skills and the ability to work independently.</li><li>Ability to lift a minimum of 50 pounds.</li><li>Proficiency in professional and Business English (written and spoken).</li></ul>Work EnvironmentThis is an on-site position, requiring presence 5 days a week in a patient-facing, clinic environment. The role is focused on engaging healthcare professionals in clinical research and making clinical trials a care option for every patient.Job Type &amp; LocationThis is a Contract to Hire position based out of Los Alamitos, CA.Pay and BenefitsThe pay range for this position is $30.00 - $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 Los Alamitos,CA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Clinical Research Coordinator – Dermatology Clinic</h2><h3>About the Role</h3>We are seeking a dedicated Clinical Research Coordinator (CRC) to support dermatology clinical trials. This role is ideal for a detail‑oriented clinical research professional who enjoys patient interaction, thrives in a fast‑paced research environment, and is committed to regulatory excellence and ethical research standards. As a CRC, you will play a critical role in the day‑to‑day execution of multiple clinical studies, working closely with Principal Investigators, sponsors, site leadership, and research participants.<hr><h3>Key Responsibilities</h3>This role includes, but is not limited to, the following:<ul><li>Manage and oversee 11–15 active clinical trials per coordinator</li><li>Conduct 20–25 patient visits per week, ensuring protocol adherence</li><li>Lead and manage clinical trials under the direction of the Principal Investigator and Site Manager</li><li>Perform patient visits, including:<ul><li>Vital signs and ECGs</li><li>Blood and urine specimen collection (phlebotomy required)</li><li>Administration of questionnaires, diaries, and study materials</li></ul></li><li>Ensure strict compliance with GCP, FDA regulations, HIPAA, OSHA, and SOPs</li><li>Accurately maintain case report forms (CRFs) and cross‑reference medical records for completeness and regulatory compliance</li><li>Collect, enter, and manage clinical data while maintaining confidentiality</li><li>Monitor study participants for safety, compliance, and protocol adherence</li><li>Manage investigational products, including receiving, dispensing, storage, and drug accountability</li><li>Coordinate with laboratories to process, ship, and review investigational samples and reports</li><li>Actively participate in patient recruitment and screening</li><li>Maintain well‑organized regulatory binders and study documentation</li><li>Ensure all required study supplies and equipment are available and functioning</li></ul><hr><h3>Required Skills &amp; Qualifications</h3><ul><li>Previous experience conducting clinical trials, including participant recruitment and regulatory compliance</li><li>Strong knowledge of Good Clinical Practices (GCP) and FDA regulations</li><li>Phlebotomy experience (certification strongly preferred)</li><li>Ability to manage multiple studies simultaneously while meeting deadlines</li><li>Excellent organizational, communication, and documentation skills</li><li>Commitment to ethical research practices and patient care</li></ul>Job Type &amp; LocationThis is a Contract to Hire 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 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator who will play a pivotal role in conducting a variety of clinical trials. This position requires patient-facing experience and a commitment to supporting groundbreaking research in a dynamic environment.Responsibilities<ul><li>Conduct pre-screening and chart review of patients.</li><li>Manage data and patient records efficiently.</li><li>Ensure compliance with Good Clinical Practice (GCP) guidelines.</li><li>Coordinate patient recruitment and enrollment processes.</li><li>Obtain informed consent from study participants.</li><li>Oversee clinical trials and ensure accurate data management.</li></ul>Essential Skills<ul><li>Minimum two years of clinical research experience in a patient-facing role.</li><li>Familiarity with the person systems.</li><li>Experience in running multiple clinical trials.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's Degree with two years of clinical research experience.</li><li>Alternatively, a high school diploma with 8 years of clinical research experience.</li><li>High school diploma with 6 years of clinical research experience plus a CRC certification from SoCRA or ACRP.</li></ul>Work EnvironmentThe role offers a combination of office and hospital/outpatient surgery settings. It is a fast-paced environment with a high volume of industry and investigator studies. The position allows for a hybrid work schedule, with the potential to work two days from home after manager approval. The campus is large and bustling, providing a stimulating work atmosphere.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 - $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 hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research Coordinator - Patient Data Entry ExperienceJob DescriptionJoin a dynamic team dedicated to advancing clinical and translational research within a specific Division. This role involves assisting with study coordination, patient recruitment, and enrollment for investigator-initiated and multi-center research studies. You will work directly with study physicians, research coordinators, project managers, and other research staff to support high-profile studies in drug trials, including those treating Parkinson's disease.Responsibilities<ul><li>Assist with study coordination and recruitment for various research projects.</li><li>Conduct patient recruitment and enrollment for clinical studies.</li><li>Perform screening visits and consent participants for studies.</li><li>Process and ship laboratory samples.</li><li>Enter data into research databases accurately.</li><li>Escort participants to testing and procedure areas.</li><li>Work closely with study physicians and other research staff.</li></ul>Essential Skills<ul><li>Experience in clinical research, patient recruitment, and enrollment.</li><li>Proficiency in chart review and data entry.</li><li>Ability to pre-screen patients effectively.</li><li>Knowledge of Good Clinical Practice (GCP).</li></ul>Additional Skills &amp; Qualifications<ul><li>1-2 years of related experience or equivalent combination of education and experience.</li></ul>Work EnvironmentOur facility is located at the northwest corner of 9th and Pine streets, easily accessible by public transport, including a short walk from PATCO and SEPTA stations. Parking is available nearby. Initially, the role requires on-site presence, with the flexibility to work from home one day a week for the first four months, increasing to two days thereafter, provided it does not interfere with responsibilities. The work is fulfilling, with opportunities to engage in studies for diseases without cures, offering significant personal and professional satisfaction. The team is diverse, well-resourced, and collaborative, with a strong support system in place.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 - $29.00/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 Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research CoordinatorJob DescriptionThe Clinical Research Coordinator will work directly with patients during visits, collaborating with research nurses as needed. Support will be provided by data and regulatory teams, requiring only a basic understanding of those functions. The position involves working within a disease-specific team, potentially the Neuro Oncology team, participating in recruitment activities, such as referrals, tumor board discussions, and new consults. Responsibilities include conducting chart reviews and supporting multiple studies without leading or owning any single study.Responsibilities<ul><li>Conduct patient visits and work directly with research nurses.</li><li>Participate in patient recruitment and inclusion/exclusion processes.</li><li>Perform chart reviews.</li><li>Support multiple studies within the team.</li></ul>Essential Skills<ul><li>Clinical research experience, with at least one year of patient-facing experience.</li><li>Patient recruitment and consent processes.</li><li>Bachelor's degree.</li><li>Clinical research certification.</li><li>Phase 1 clinical trials experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology is preferred.</li><li>Clinical research certification is a plus.</li></ul>Work EnvironmentThe work schedule will start between 7:00-9:00 am, with 8-hour shifts. Work is onsite at The Henry Ford Cancer Center every day for the first three months, with the option to work from home one day a week thereafter. The role offers opportunities to learn and grow, access to internal training, and potential for higher pay with SOCRA or ACRP certification. The new leadership is establishing structured onboarding, training, and development, providing defined roles and manageable workloads to allow specialization.Job Type &amp; LocationThis is a Contract to Hire position based out of Detroit, MI.Pay and BenefitsThe pay range for this position is $27.00 - $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 hybrid position in Detroit,MI.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Research CoordinatorJob DescriptionJoin our dynamic team as a Research Coordinator, where you will coordinate clinical trials in accordance with FDA and GCP guidelines. You will play a crucial role in scheduling patient visits and maintaining high-quality data entry in the Electronic Data Capture (EDC) system. Collaborate closely with the marketing coordinator for effective subject recruitment, and input visit data into the Clinical Trial Management System (CTMS) for accurate tracking of patient visits and procedures.Responsibilities<ul><li>Coordinate trials per FDA and GCP guidelines.</li><li>Schedule patient visits and manage trial data in the Electronic Data Capture (EDC) system, ensuring quality control.</li><li>Collaborate with the marketing coordinator for subject recruitment.</li><li>Input visit data into the Clinical Trial Management System (CTMS) to track patient visits and completed procedures.</li><li>Process required lab specimens, label vials, and accurately complete requisitions for storage and shipment according to study protocol.</li><li>Prepare and maintain research study files, and compile, collate, and submit study information within established deadlines.</li></ul>Required Skills &amp; Experience<ul><li>Pre-screening patients</li><li>Experience in clinical research and clinical trials</li><li>Patient recruitment</li><li>At least 1 year of clinical research experience</li></ul>Additional Skills &amp; Qualifications<ul><li>BS/BA in life sciences, biology, or educational equivalent, and/or relevant work experience in a clinical environment or medical setting.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li><li>Basic knowledge of medical terminology.</li><li>Proficiency in MS Windows and Office applications like Access, Outlook, Excel, and Word.</li><li>Ability to quickly learn industry-specific software and experience with social media platforms and interoffice software.</li></ul>Work EnvironmentThis position is based in Tulsa, Oklahoma, where you will be a part of a best-in-class clinical research site contributing to the development of new medications. The work involves trials related to Crohn's, Lupus, and Dermatitis.Job Type &amp; LocationThis is a Contract to Hire position based out of Tulsa, OK.Pay and BenefitsThe pay range for this position is $24.04 - $26.44/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 Tulsa,OK.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Study CoordinatorJob DescriptionThe Study Coordinator is responsible for the coordination and administration of clinical studies under the guidance of the Director of Study Management and the Medical Director/Principal Investigator. This role involves developing, implementing, and coordinating research and administrative procedures essential for the successful management of clinical studies. The Study Coordinator will perform various administrative duties requiring analysis, sound judgment, and a comprehensive understanding of study-specific protocols.Responsibilities<ul><li>Maintain required records of study activity including study logs, case report forms, and regulatory forms.</li><li>Schedule volunteers for appointments, procedures, and inpatient stays as required by study protocols.</li><li>Assess eligibility of potential volunteers through interviews, reviews of medical records, and discussions with Investigators and Research Associates.</li><li>Communicate with the Laboratory and Investigators regarding lab procedures and findings.</li><li>Educate study volunteers on study procedures such as diary completion, electronic devices, and expected outcomes in a professional and accountable manner following protocol requirements.</li><li>Ensure training and documentation are completed for protocol amendments, ICFs, and updated guidelines.</li><li>Communicate ongoing updates, amendments, and changes with Nursing staff.</li><li>Maintain communication with Investigators regarding study progress, safety issues, and other important information.</li><li>Maintain contact with sponsors/CROs and respond in a timely manner while coordinating site visits.</li><li>Exhibit professional communication and a collaborative work ethic with CRAs at site visits.</li><li>Order and track supplies or devices necessary for study completion.</li><li>Prepare study-related source documentation according to protocol and system guidelines, collaborating with the QA department to make necessary changes.</li><li>Record adverse events and discuss with Investigators regarding the reporting of events to oversight agencies.</li><li>Track enrollment status of volunteers and documentation in the Clinical Conductor system.</li><li>Perform specific protocol procedures such as interviewing volunteers, taking vital signs, and performing electrocardiograms.</li><li>Prepare for or participate in quality assurance audits conducted by sponsors, federal agencies, or specially designated review groups.</li><li>Adhere to safety and privacy regulations.</li><li>Perform other duties as assigned.</li></ul>Essential Skills<ul><li>Experience in chart review, pre-screening patients, clinical research, clinical trial, and patient recruitment.</li><li>Must be an RN or LPN.</li><li>High school diploma or GED is required; a Bachelor’s degree in Science is preferred.</li><li>3 to 5 years of experience in a clinical research setting or related work environment is preferred.</li><li>Basic understanding of regulations governing clinical research such as CFR, GCP, and HIPAA.</li><li>Solid understanding of statutes and guidelines relevant to regulatory affairs in clinical research.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiarity with or ability to learn clinical trial management system software.</li></ul>Work EnvironmentThe work environment is office-based, providing a professional setting conducive to clinical research activities.Job Type &amp; LocationThis is a Permanent position based out of Lenexa, KS.Pay and BenefitsThe pay range for this position is $65000.00 - $70000.00/yr.Direct Placement. Direct Placement. Direct Placement.Direct Placement.Direct Placement.Direct Placement.Workplace TypeThis is a fully onsite position in Lenexa,KS.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2>Job Title: Oncology Clinical Research Coordinator</h2>Job DescriptionThis role involves working directly with patients and conducting patient visits. The Clinical Research Coordinator will collaborate closely with research nurses and will have the support of Data and Regulatory teams. While a basic understanding of these functions is required, the Coordinator will not be responsible for them. The position involves working within teams divided by disease group, potentially including Phase 1 clinical trials.Responsibilities<ul><li>Conduct patient visits and work directly with patients.</li><li>Collaborate with research nurses as needed during patient visits.</li><li>Participate in recruitment activities using methods such as referrals, tumor board, and new consults.</li><li>Conduct chart reviews to support studies.</li><li>Support all studies within the team, without owning or leading any specific study.</li><li>Manage a patient load of no more than 10 patients a week, with patient visits varying by team and study phase.</li></ul>Essential Skills<ul><li>At least one year of clinical trial experience, including patient-facing roles, consenting patients, and conducting patient visits.</li><li>Experience in oncology or other complex therapeutic area.</li><li>Bachelor's Degree.</li><li>Experience with Phase 1 clinical trials.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of Detroit, MI.Pay and BenefitsThe pay range for this position is $27.00 - $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 hybrid position in Detroit,MI.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research CoordinatorJob DescriptionWe are seeking a dedicated Clinical Research Coordinator to oversee and manage diagnostic breast imaging studies. The role involves preparing and processing all Institutional Review Board (IRB) documents and coordinating essential documentation required by sponsors or CROs. This position ensures the accurate reporting of adverse events in compliance with relevant regulations and protocols.Responsibilities<ul><li>Coordinate diagnostic breast imaging studies.</li><li>Prepare and process initial submissions, amendments, and continuing reviews through the Institutional Review Board (IRB) and other regulatory bodies.</li><li>Organize and maintain all documentation required by sponsors or CROs, including case report forms, source documentation, study and regulatory binders, and subject binders.</li><li>Ensure proper reporting of serious and non-serious adverse events to the Sponsor and all applicable institutional or study-related committees and personnel, such as the IRB, DSMC, DSMB/Medical Monitor.</li></ul>Essential Skills<ul><li>Bachelor of Science degree.</li><li>2 to 3 years of clinical research experience or an equivalent combination of education and experience.</li><li>Prior experience with clinical trials required.</li><li>Proficiency in clinical research, data management, patient recruitment, and enrollment.</li><li>Experience with chart review, data entry, and screening.</li></ul>Additional Skills &amp; Qualifications<ul><li>Strong organizational and communication skills.</li><li>Ability to work collaboratively in a team environment.</li></ul>Work EnvironmentThis position offers a hybrid schedule, with on-site work required. Our mission is to provide advanced breast imaging technology for precise detection and diagnosis of breast diseases. The work environment supports high-quality interventional breast procedures, including stereotactic, ultrasound-guided, and MRI-guided biopsies.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 - $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 hybrid position in Philadelphia,PA.Application DeadlineThis position is anticipated to close on Feb 28, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator*Must Have Oncology experience*Job DescriptionThe Clinical Research Coordinator (Non-RN) is integral to the execution of research studies, trials, and programs. This role involves patient screening, assessing eligibility, and coordinating care and follow-up for volunteers involved in research. Key activities include recruiting and consenting research participants, providing exceptional patient service during clinical trials, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure regulatory and protocol compliance.Responsibilities<ul><li>Execute and coordinate the informed consent process for research institute participants across multiple locations, necessitating travel between sites and research laboratories, and/or the use of technology.</li><li>Oversee all aspects of research including patient screening, assessing eligibility, and coordinating participation and follow-up of volunteers in research studies, trials, and programs.</li><li>Recruit and consent research participants for therapeutic areas served.</li><li>Provide concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (blood, tissue) and maintain HIPAA-protected database linking patient information to biospecimens used in research; perform patient chart reviews and data collection.</li><li>Collaborate with clinical research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure regulatory and protocol compliance.</li><li>Work with assistant clinical coordinators to ensure compliant data entry and data mining into registries, patient records, and research-specific databases.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and other control documents.</li><li>Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.</li><li>Collaborate with clinical research supervisors and staff to implement SOPs for the research division to meet standards, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.</li></ul>Essential Skills<ul><li>Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously in an organized and timely manner.</li><li>Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.</li><li>Effective communication skills with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem-solving, capable of obtaining and analyzing facts and applying sound judgment.</li><li>Ability to accept direction and respond to the changing needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet knowledge and skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field.</li><li>Associates degree in Healthcare Administration, Research, or related field with two years of experience.</li><li>Graduate of an accredited allied health certificate program with four years of clinical research or healthcare experience.</li><li>Oncology Experience</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Kissimmee, FL.Pay and BenefitsThe pay range for this position is $65000.00 - $78000.00/yr.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 Kissimmee,FL.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator (Contract Position)Contract Duration: Open-ended (estimated until end of May 2026)Schedule: 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. This contractor will function as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities. 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>Create and maintain source documents and ensure all study records are complete, up-to-date, and audit-ready.</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 Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator (30 Hours)

Job Title: Clinical Research Coordinator IIJob DescriptionThe Clinical Research Coordinator II will conduct clinical research and work independently on progressively more complex projects and assignments. The role involves independently managing significant and key aspects of a large study or all aspects of one or more small research studies.Responsibilities<ul><li>Oversee subject recruitment and study enrollment goals, determining effective strategies for promoting and recruiting research participants and retaining participants in long-term clinical trials.</li><li>Manage data for research projects by developing systems to organize, collect, report, and monitor data collection, and extract, analyze, and interpret data.</li><li>Develop project schedules, targets, measurements, and accountabilities as assigned, leading team meetings and preparing or approving minutes.</li><li>Supervise, train, and mentor new staff or students, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and providing instruction on project work.</li><li>Audit operations, including laboratory procedures, to ensure compliance with applicable regulations and provide leadership in identifying and implementing corrective actions and processes.</li><li>Monitor Institutional Review Board submissions, respond to requests and questions, and collaborate with principal investigators and study sponsors.</li><li>Provide leadership in determining, recommending, and implementing improvements to policies and processes, defining best practices.</li><li>Develop study budgets with staff and principal investigator, identifying standard of care versus study procedures, tracking patient and study-specific milestones, and invoicing sponsors according to study contracts.</li><li>Ensure regulatory compliance by regularly inspecting study documents and ensuring ongoing regulatory compliance.</li><li>Work with principal investigators 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 of experience as a Clinical Research Coordinator, specifically in oncology and complex clinical trials such as cardio, CAR-T, and transplant.</li><li>Experience with interventional sponsored studies, specifically treatment trials within Phase I-II.</li><li>Hands-on experience working with patients in treatment trials.</li><li>Experience in coordinator site roles, not in pharma, CRO, or lab research.</li><li>Proficiency with EPIC and experience in chart review, pre-screening patients, and EDC.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology treatment Phase I trials.</li><li>Experience with patient-facing study flows and ability to conduct data work from home after training.</li></ul>Work EnvironmentThis role offers a hybrid work environment with four days onsite and one potential flexible day. The opportunity to work with one of the most renowned academic institutions in the US is presented, with a principal investigator who is very hands-on with contractors.Job Type &amp; LocationThis is a Contract to Hire position based out of Palo Alto, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 Palo Alto,CA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator II

Job Title: Clinical Research Coordinator IIJob DescriptionThe Clinical Research Coordinator II will conduct clinical research and work independently on progressively more complex projects and assignments. The role involves independently managing significant and key aspects of a large study or all aspects of one or more small research studies.Responsibilities<ul><li>Oversee subject recruitment and study enrollment goals, determining effective strategies for promoting and recruiting research participants and retaining participants in long-term clinical trials.</li><li>Manage data for research projects by developing systems to organize, collect, report, and monitor data collection, and extract, analyze, and interpret data.</li><li>Develop project schedules, targets, measurements, and accountabilities as assigned, leading team meetings and preparing or approving minutes.</li><li>Supervise, train, and mentor new staff or students, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and providing instruction on project work.</li><li>Audit operations, including laboratory procedures, to ensure compliance with applicable regulations and provide leadership in identifying and implementing corrective actions and processes.</li><li>Monitor Institutional Review Board submissions, respond to requests and questions, and collaborate with principal investigators and study sponsors.</li><li>Provide leadership in determining, recommending, and implementing improvements to policies and processes, defining best practices.</li><li>Develop study budgets with staff and principal investigator, identifying standard of care versus study procedures, tracking patient and study-specific milestones, and invoicing sponsors according to study contracts.</li><li>Ensure regulatory compliance by regularly inspecting study documents and ensuring ongoing regulatory compliance.</li><li>Work with principal investigators 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 of experience as a Clinical Research Coordinator, specifically in oncology and complex clinical trials such as cardio, CAR-T, and transplant.</li><li>Experience with interventional sponsored studies, specifically treatment trials within Phase I-II.</li><li>Hands-on experience working with patients in treatment trials.</li><li>Experience in coordinator site roles, not in pharma, CRO, or lab research.</li><li>Proficiency with EPIC and experience in chart review, pre-screening patients, and EDC.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology treatment Phase I trials.</li><li>Experience with patient-facing study flows and ability to conduct data work from home after training.</li></ul>Work EnvironmentThis role offers a hybrid work environment with four days onsite and one potential flexible day. The opportunity to work with one of the most renowned academic institutions in the US is presented, with a principal investigator who is very hands-on with contractors.Job Type &amp; LocationThis is a Contract position based out of Palo Alto, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 Palo Alto,CA.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research Coordinator IIJob DescriptionThe Clinical Research Coordinator II will conduct clinical research and work independently on progressively more complex projects and assignments. The role involves independently managing significant and key aspects of a large study or all aspects of one or more small research studies.Responsibilities<ul><li>Oversee subject recruitment and study enrollment goals, determining effective strategies for promoting and recruiting research participants and retaining participants in long-term clinical trials.</li><li>Manage data for research projects by developing systems to organize, collect, report, and monitor data collection, and extract, analyze, and interpret data.</li><li>Develop project schedules, targets, measurements, and accountabilities as assigned, leading team meetings and preparing or approving minutes.</li><li>Supervise, train, and mentor new staff or students, potentially including hiring, preparing or assisting with the preparation of performance evaluations, and providing instruction on project work.</li><li>Audit operations, including laboratory procedures, to ensure compliance with applicable regulations and provide leadership in identifying and implementing corrective actions and processes.</li><li>Monitor Institutional Review Board submissions, respond to requests and questions, and collaborate with principal investigators and study sponsors.</li><li>Provide leadership in determining, recommending, and implementing improvements to policies and processes, defining best practices.</li><li>Develop study budgets with staff and principal investigator, identifying standard of care versus study procedures, tracking patient and study-specific milestones, and invoicing sponsors according to study contracts.</li><li>Ensure regulatory compliance by regularly inspecting study documents and ensuring ongoing regulatory compliance.</li><li>Work with principal investigators 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 of experience as a Clinical Research Coordinator, specifically in oncology and complex clinical trials such as cardio, CAR-T, and transplant.</li><li>Experience with interventional sponsored studies, specifically treatment trials within Phase I-II.</li><li>Hands-on experience working with patients in treatment trials.</li><li>Experience in coordinator site roles, not in pharma, CRO, or lab research.</li><li>Proficiency with EPIC and experience in chart review, pre-screening patients, and EDC.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in oncology treatment Phase I trials.</li><li>Experience with patient-facing study flows and ability to conduct data work from home after training.</li></ul>Work EnvironmentThis role offers a hybrid work environment with four days onsite and one potential flexible day. The opportunity to work with one of the most renowned academic institutions in the US is presented, with a principal investigator who is very hands-on with contractors.Job Type &amp; LocationThis is a Contract position based out of Palo Alto, CA.Pay and BenefitsThe pay range for this position is $35.00 - $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 Palo Alto,CA.Application DeadlineThis position is anticipated to close on Feb 21, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

<h2 style="text-align:center;">Job Title: Clinical Research Coordinator II</h2>Job DescriptionThe Clinical Research Coordinator (Non-RN) is integral to the execution of research studies, trials, and programs. This role involves patient screening, assessing eligibility, and coordinating care and follow-up for volunteers involved in research. Key activities include recruiting and consenting research participants, providing exceptional patient service during clinical trials, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure regulatory and protocol compliance.Responsibilities<ul><li>Execute and coordinate the informed consent process for research institute participants across multiple locations, necessitating travel between sites and research laboratories, and/or the use of technology.</li><li>Oversee all aspects of research including patient screening, assessing eligibility, and coordinating participation and follow-up of volunteers in research studies, trials, and programs.</li><li>Recruit and consent research participants for therapeutic areas served.</li><li>Provide concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (blood, tissue) and maintain HIPAA-protected database linking patient information to biospecimens used in research; perform patient chart reviews and data collection.</li><li>Collaborate with clinical research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices to ensure regulatory and protocol compliance.</li><li>Work with assistant clinical coordinators to ensure compliant data entry and data mining into registries, patient records, and research-specific databases.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and other control documents.</li><li>Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.</li><li>Collaborate with clinical research supervisors and staff to implement SOPs for the research division to meet standards, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.</li></ul>Essential Skills<ul><li>Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously in an organized and timely manner.</li><li>Knowledge of HIPAA data protection and patient advocacy or similar awareness of ethical treatment of participants in research.</li><li>Effective communication skills with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem-solving, capable of obtaining and analyzing facts and applying sound judgment.</li><li>Ability to accept direction and respond to the changing needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet knowledge and skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field.</li><li>Associates degree in Healthcare Administration, Research, or related field with two years of experience.</li><li>Graduate of an accredited allied health certificate program with four years of clinical research or healthcare experience.</li></ul>Work EnvironmentThe work environment is office-based, with a focus on collaboration and compliance with clinical research standards.Please send your resume and 2-3 professional references to mscherlacher @actalentservices.com for next steps.Job Type &amp; LocationThis is a Permanent position based out of Orlando, FL.Pay and BenefitsThe pay range for this position is $64480.00 - $74880.00/yr.country, this unwavering belief binds us together. Across every office, exam and patient room, we're committed to providing individualized, holistic care. This is our Christian mission, and it inspires us to help make communities healthier and happier.

All the benefits and perks you need for you and your family:

Benefits from Day One

Paid Days Off from Day One

Career Development

Mental Health Resources and Support

Pet Insurance*Workplace TypeThis is a fully onsite position in Orlando,FL.Application DeadlineThis position is anticipated to close on Feb 21, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Coordinator II (TRI)

Clinical Research Infusion NurseAs an Oncology Infusion Research Nurse, you will manage the specialized care of cancer patients enrolled in clinical trials. This role blends your hands‑on infusion expertise with the unique responsibilities of clinical research, including:<ul><li>Protocol Compliance &amp; Safety: Ensuring strict adherence to clinical trial protocols, FDA regulations, and ICH/GCP guidelines to safeguard patient welfare.</li><li>Infusion Administration: Delivering chemotherapy, biotherapy, and investigational agents while applying advanced knowledge of oncology medications and side‑effect management.</li><li>Patient Monitoring: Conducting detailed clinical assessments, monitoring for adverse reactions, and evaluating patient toxicity levels per protocol requirements.</li><li>Data Collection &amp; Management: Documenting source data and completing Case Report Forms (CRFs) with accuracy and attention to detail.</li><li>Study Coordination: Collaborating closely with Principal Investigators, research coordinators, and pharmacy teams to ensure smooth and compliant study execution.</li><li>Education &amp; Support: Providing guidance and education to patients and families regarding study expectations, treatment processes, and potential side effects.</li></ul> Required QualificationsTo be considered for this role, candidates must meet the following criteria:<ul><li>Active Florida RN license (required)</li><li>Chemotherapy infusion experience and proficiency with PIVs</li><li>Oncology experience (OCN certification preferred)</li><li>Active ACLS and BLS certifications</li></ul> ScheduleOnsite 4 days 10-hour shifts ; schedule made 6 weeks in advanceJob Type &amp; LocationThis is a Permanent position based out of Orlando, FL.Pay and BenefitsThe pay range for this position is $83200.00 - $99840.00/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 Feb 21, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Infusion Nurse

Clinical Research Infusion NurseAs an Oncology Infusion Research Nurse, you will manage the specialized care of cancer patients enrolled in clinical trials. This role blends your hands‑on infusion expertise with the unique responsibilities of clinical research, including:<ul><li>Protocol Compliance &amp; Safety: Ensuring strict adherence to clinical trial protocols, FDA regulations, and ICH/GCP guidelines to safeguard patient welfare.</li><li>Infusion Administration: Delivering chemotherapy, biotherapy, and investigational agents while applying advanced knowledge of oncology medications and side‑effect management.</li><li>Patient Monitoring: Conducting detailed clinical assessments, monitoring for adverse reactions, and evaluating patient toxicity levels per protocol requirements.</li><li>Data Collection &amp; Management: Documenting source data and completing Case Report Forms (CRFs) with accuracy and attention to detail.</li><li>Study Coordination: Collaborating closely with Principal Investigators, research coordinators, and pharmacy teams to ensure smooth and compliant study execution.</li><li>Education &amp; Support: Providing guidance and education to patients and families regarding study expectations, treatment processes, and potential side effects.</li></ul> Required QualificationsTo be considered for this role, candidates must meet the following criteria:<ul><li>Active Florida RN license (required)</li><li>Chemotherapy infusion experience and proficiency with PIVs</li><li>Oncology experience (OCN certification preferred)</li><li>Active ACLS and BLS certifications</li></ul> ScheduleOnsite 4 days 10-hour shifts ; schedule made 6 weeks in advanceJob Type &amp; LocationThis is a Permanent position based out of Orlando, FL.Pay and BenefitsThe pay range for this position is $83200.00 - $99840.00/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 Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research Manager - Oncology Job DescriptionThe Clinical Research Site Manager is responsible for overseeing the daily operations of clinical research at the site, ensuring that all activities are carried out in accordance with applicable regulations and company standards. Responsibilities<ul><li>Coordinate study activities, including protocol feasibility assessments, budgeting, recruitment, screening, enrollment, and participant retention.</li><li>Manage clinical trial systems (CTMS), study documentation, data collection, and regulatory paperwork to ensure smooth study execution and compliance.</li><li>Regularly meet with leadership to review study metrics, financials, and regulatory requirements, ensuring proactive management of operational aspects.</li><li>Lead and manage a team of Clinical Research Coordinators, Nurses, and Assistants, including hiring, training, mentoring, and performance evaluations.</li><li>Develop and implement SOPs and quality control measures to maintain high standards of research operations.</li><li>Address staff performance and provide constructive feedback, working closely with HR and leadership to resolve any issues.</li><li>Collaborate with leadership and investigators to assess new research opportunities and initiatives.</li><li>Ensure effective communication within the team and resolve any operational challenges in a constructive manner.</li><li>Provide staff coverage as needed and support in various office-related tasks.</li></ul>Essential Skills<ul><li>Demonstrated experience in clinical trials and familiarity with industry regulations.</li><li>Strong leadership and supervisory skills with the ability to motivate and mentor staff.</li><li>Excellent organizational skills with the capacity to manage multiple priorities and meet deadlines.</li><li>Proficient in interpreting policies, processes, and regulatory guidelines.</li><li>Strong problem-solving and decision-making abilities.</li><li>Effective communication skills, both verbal and written.</li><li>Ability to build and maintain professional relationships with internal and external stakeholders.</li><li>High proficiency in Microsoft Office and general office technologies.</li><li>Bachelor's Degree required.</li></ul>Additional Skills &amp; Qualifications<ul><li>RN, Nurse Practitioner License, or PA-C, CCRP certification preferred.</li><li>Ability to always maintain confidentiality.</li></ul>Work EnvironmentFoster a positive, team-oriented work environment that prioritizes safety, respect, and collaboration. Ensure all activities adhere to company policies, Standard Operating Procedures (SOPs), and industry regulations. Travel to other research locations when necessary.Job Type &amp; LocationThis is a Permanent position based out of Cerritos, CA.Pay and BenefitsThe pay range for this position is $100000.00 - $130000.00/yr.Benefits through corporate.Workplace TypeThis is a fully onsite position in Cerritos,CA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Manager

Job Title: Clinical Research ManagerJob DescriptionThe Clinical Research Site Manager is responsible for overseeing the daily operations of clinical research at the site, ensuring that all activities are carried out in accordance with applicable regulations and company standards. This role involves managing research staff, including Clinical Research Coordinators, Nurses, and Assistants, maintaining regulatory compliance, and ensuring the timely execution of studies. The manager also serves as a key liaison between the research team, leadership, and external partners.Responsibilities<ul><li>Oversee day-to-day clinical research operations under the guidance of the Vice President of Clinical Research, ensuring efficient workflows and high-quality service delivery.</li><li>Coordinate study activities, including protocol feasibility assessments, budgeting, recruitment, screening, enrollment, and participant retention.</li><li>Manage clinical trial systems (CTMS), study documentation, data collection, and regulatory paperwork to ensure smooth study execution and compliance.</li><li>Regularly meet with leadership to review study metrics, financials, and regulatory requirements, ensuring proactive management of operational aspects.</li><li>Lead and manage a team of Clinical Research Coordinators, Nurses, and Assistants, including hiring, training, mentoring, and performance evaluations.</li><li>Develop and implement SOPs and quality control measures to maintain high standards of research operations.</li><li>Address staff performance and provide constructive feedback, working closely with HR and leadership to resolve any issues.</li><li>Collaborate with leadership and investigators to assess new research opportunities and initiatives.</li><li>Ensure effective communication within the team and resolve any operational challenges in a constructive manner.</li><li>Provide staff coverage as needed and support in various office-related tasks.</li><li>Travel to other research locations when necessary.</li></ul>Essential Skills<ul><li>Demonstrated experience in clinical trials and familiarity with industry regulations.</li><li>Strong leadership and supervisory skills with the ability to motivate and mentor staff.</li><li>Excellent organizational skills with the capacity to manage multiple priorities and meet deadlines.</li><li>Proficient in interpreting policies, processes, and regulatory guidelines.</li><li>Strong problem-solving and decision-making abilities.</li><li>Effective communication skills, both verbal and written.</li><li>Ability to build and maintain professional relationships with internal and external stakeholders.</li><li>High proficiency in Microsoft Office and general office technologies.</li><li>Bachelor's Degree required.</li></ul>Additional Skills &amp; Qualifications<ul><li>RN, Nurse Practitioner License, or PA-C, CCRP certification preferred.</li><li>Ability to always maintain confidentiality.</li></ul>Work EnvironmentFoster a positive, team-oriented work environment that prioritizes safety, respect, and collaboration. Ensure all activities adhere to company policies, Standard Operating Procedures (SOPs), and industry regulations. Travel to other research locations when necessary.Job Type &amp; LocationThis is a Permanent position based out of Fountain Valley, CA.Pay and BenefitsThe pay range for this position is $100000.00 - $130000.00/yr.Benefits through corporate.Workplace TypeThis is a fully onsite position in Fountain Valley,CA.Application DeadlineThis position is anticipated to close on Feb 26, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research Navigator Job DescriptionWe are seeking a dedicated Clinical Research Navigator to join our dynamic team. The successful candidate will play a crucial role in coordinating clinical trials, ensuring that patients meet the necessary criteria for study participation, and managing communication between sponsors, physicians, and patients. This position offers a fast-paced environment with opportunities to learn and collaborate closely with medical professionals.Responsibilities<ul><li>Meet with patients to determine study eligibility.</li><li>Coordinate with the Navigator to request study slots from sponsors.</li><li>Read and interpret inclusion and exclusion criteria from protocols and electronic medical records (EMR) efficiently.</li><li>Serve as a liaison between patients, sponsors, and physicians, facilitating effective communication through EPIC, calls, emails, etc.</li><li>Track and manage waitlists and spreadsheets related to clinical trials.</li><li>Provide timely updates to sponsors and Principal Investigators (PIs) regarding patient status and care.</li><li>Adjust communication strategies to meet the expectations of various sponsors and PIs.</li><li>Manage responsibilities across 16-25 studies in a fast-paced environment.</li></ul>Essential Skills<ul><li>Experience in clinical research, particularly in oncology and clinical trials.</li><li>Proficiency in pre-screening patients and conducting chart reviews.</li><li>Understanding of drug trials and Phase 1 Clinical Trials.</li><li>Ability to interpret and apply inclusion and exclusion criteria.</li><li>Strong communication skills for effective liaison work between physicians, patients, and sponsors.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience as a Research Nurse is a plus.</li><li>Previous Phase 1 oncology experience is highly beneficial.</li></ul>Work EnvironmentThe role is primarily onsite. There is flexibility to work from home occasionally, including on Fridays. This position offers a fast-paced work environment where you will have the opportunity to collaborate closely with physicians, medical directors, and sponsors.Job Type &amp; LocationThis is a Contract to Hire position based out of Indianapolis, IN.Pay and BenefitsThe pay range for this position is $28.00 - $38.00/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 Indianapolis,IN.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Navigator

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study. The Clinical Research Nurse serves as a resource to 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 new clinical trial protocols.</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 protocol 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>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>Obtain informed consent for both therapeutic and non-therapeutic studies in accordance with IRB, GCP, and institutional policies.</li><li>Serve as a link between patients and all other members of the research team, addressing challenges with protocol completion and adherence.</li><li>Ensure protocol-specific orders are executed accurately, coordinating continuity of protocol-specified procedures between disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and deliver high-quality, compassionate oncology nursing care.</li><li>Collaborate with medical system staff to ensure coordinated and timely services for patients.</li><li>Grade adverse events using protocol-referenced NCI common toxicity criteria, provide informal teaching/coaching to clinicians, and complete SAE forms.</li><li>Assist in monitoring visits, audits, and providing responses to sponsor's queries.</li><li>Maintain research records for screened and enrolled patients, ensuring adherence to regulations and guidelines.</li></ul>Essential Skills<ul><li>Experience and comfortability communicating with patients.</li><li>Clinical research coordinator experience (1-3 years).</li><li>Proficiency in computerized systems (e.g., Word, Excel).</li><li>Excellent communication and interpersonal skills.</li><li>Detail-oriented with excellent organizational skills.</li><li>Ability to maximize resources and be resourceful.</li></ul>Additional Skills &amp; Qualifications<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; 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>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>Job Type &amp; LocationThis is a Contract to Hire position based out of Somerville, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $55.00/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 Somerville,NJ.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Nurse

<h2 style="text-align:center;">Job Title: Clinical Research Nurse</h2>Job DescriptionThe Clinical Research Nurse plays a crucial role in the research efforts of the institute. This position involves planning, coordinating, evaluating, and performing nursing care for research participants, as well as collecting data for assigned research projects. The role requires adherence to study-specific protocol guidelines and involves communication with Principal Investigators, Sub-Investigators, Clinical Research Leads, and other support staff. The Clinical Research Nurse is dedicated to patient advocacy while conducting industry-sponsored and investigator-initiated clinical trials in compliance with trial protocols, FDA regulations, and ICH/GCP guidelines.Responsibilities<ul><li>Deliver safe nursing care with respect and dignity for all participants.</li><li>Maintain clinical competencies such as physical assessment, phlebotomy, and IV insertion.</li><li>Practice Universal Precautions and understand HIPAA regulations.</li><li>Ensure clinical spaces are clean and prepared, performing set-up and turnover procedures as needed.</li><li>Participate in training programs to maintain licensure.</li><li>Communicate effectively with healthcare team members, patients, investigators, and sponsors.</li><li>Review and adhere to IRB approved informed consent documents, advocating for patient rights and safety.</li><li>Manage multiple clinical trial protocols, ensuring accurate and timely documentation.</li><li>Securely manage records, study medications, and test articles.</li><li>Promote PI oversight and report deviations or issues relevant to trial integrity and subject safety.</li><li>Coordinate the work of support staff, laboratory technicians, and assistants to ensure adherence to protocols.</li></ul>Essential Skills<ul><li>Proficiency in clinical trial processes and data collection.</li><li>Experience in oncology, dose calculations, consenting, and dosing.</li><li>Knowledge of diabetes, clinical research, and GCP.</li><li>Ability to perform EKG and other clinical tasks within the scope of practice.</li><li>Minimum of 2 years of clinical research experience.</li><li>Current, active State of Florida license as a Registered Nurse.</li><li>BLS certification.</li></ul>Additional Skills &amp; Qualifications<ul><li>Associate degree in Nursing.</li><li>Skills in clinical competencies such as physical assessment, phlebotomy, and IV insertion.</li><li>Ability to assist physicians and CRNs with procedures and study requirements.</li><li>Adaptability to integrate into various clinical settings as needed.</li></ul>Work EnvironmentThe position is situated in a hospital setting, requiring adherence to hospital and departmental policies, SOPs, and all applicable regulations.Job Type &amp; LocationThis is a Permanent position based out of Orlando, FL.Pay and BenefitsThe pay range for this position is $83200.00 - $98000.00/yr.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 Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research NurseDuties<ul><li>Perform all administration related to investigational products (IP), including injections, dosing, and drug mixing</li><li>Support multiple studies (not assigned to a single trial)</li><li>Assist with blood draws as needed</li><li>Collaborate with a team of Clinical Research Coordinators (CRCs) and Research Assistants (RAs)</li><li>Ensure compliance with study protocols and regulatory requirements</li></ul>Required Qualifications<ul><li>Active California RN license</li><li>MUST have a minimum of 1 year of clinical research experience</li><li>Must be licensed to mix drugs in CA (required for investigational product preparation)</li><li>IV experience</li><li>Infusion experience</li></ul>ScheduleOnsite Monday–Friday, 8:00 AM–5:00 PM (1-hour lunch break)Job Type &amp; LocationThis is a Contract to Hire position based out of Fountain Valley, CA.Pay and BenefitsThe pay range for this position is $40.00 - $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 Fountain Valley,CA.Application DeadlineThis position is anticipated to close on Mar 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Research NurseGreat opportunity to gain experience in Clinical ResearchSchedule: Fri-Sun 6pm-6am CSTJob DescriptionJoin our team as a Research Nurse where you will play a pivotal role in conducting clinical trials, ensuring the safety and welfare of study participants.Responsibilities<ul><li>Enroll patients into clinical trials, including the Informed Consent process by educating, explaining, and informing participants of study procedures.</li><li>Utilize nursing skills, knowledge, and clinical judgment to provide high-quality care for trial participants.</li><li>Use nursing assessment skills to observe participants' general well-being and identify potential adverse events.</li><li>Document adverse events and take appropriate action as needed.</li><li>Perform study-related activities such as cannulation, telemetry, holters, vital signs, ECGs, and venipuncture.</li><li>Collect and process biological samples according to the protocol and Standard Operating Procedures.</li><li>Record data in a timely, error-free manner according to the protocol and Standard Operating Procedures.</li><li>Transcribe source data onto the Case Report Form.</li></ul>Essential Skills<ul><li>Active Registered Nurse (RN) license in Wisconsin, in good standing.</li><li>Associates Degree or Bachelors Degree in Nursing (ASN or BSN).</li><li>0-3 years of nursing experience in a patient-facing setting.</li><li>Alternatively, a Licensed Practical Nurse (LPN) with 0-3 years of nursing experience, active and in good standing in Wisconsin.</li></ul>Additional Skills &amp; Qualifications<ul><li>Previous experience with clinical research is preferred.</li><li>CPR and ACLS certifications.</li></ul>Work EnvironmentThe position is based at the Phase I Clinical Research Unit in Madison, WI. The work environment is dynamic, with a focus on clinical research and the opportunity for professional growth. The organization provides extensive training in clinical research and study-specific protocolsJob Type &amp; LocationThis is a Contract to Hire position based out of MADISON, WI.Pay and BenefitsThe pay range for this position is $30.00 - $38.00/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 MADISON,WI.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Registered NurseSeeking an experienced Clinical Research Nurse with IV infusion skills and knowledge of infusion nursing practices. This role involves administering FDA-approved and investigational drugs and managing multiple studies from start to finish.Responsibilities:<ul><li>Administer study drugs and perform clinical assessments (vitals, EKGs, specimen collection).</li><li>Screen, consent, and schedule participants per protocol.</li><li>Maintain regulatory binders, source documents, and CRFs.</li><li>Report AEs, SAEs, and protocol deviations per FDA/GCP guidelines.</li><li>Manage investigational product inventory and reconciliation.</li><li>Coordinate with sponsors during site visits and audits.</li><li>Support PI during consent and study visits; train new staff.</li></ul>Qualifications:<ul><li>2+ year nursing experience</li><li>Active Georgia RN license</li><li>IV infusion experience</li><li>Phlebotomy experience</li><li>BLS certification</li><li>Bachelor’s degree in Nursing</li><li>Experience with MS Office Suite</li><li>Experience with EDC and CTMS</li><li>Experience with EMR</li></ul>Job Type &amp; LocationThis is a Permanent position based out of Atlanta, GA.Pay and BenefitsThe pay range for this position is $65000.00 - $75000.00/yr.-health insurance with medical, vision, dental
-401K
-PTOWorkplace TypeThis is a fully onsite position in Atlanta,GA.Application DeadlineThis position is anticipated to close on Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study.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 study conduct.</li><li>Perform nursing education to other disciplines for safe, effective care of enrolled patients.</li><li>Translate finalized protocol treatment plans into sample orders.</li><li>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.</li><li>Follow informed consent processes to ensure that IRB approved consent has been obtained and documented.</li><li>Provide backup support to register consented research patients and input data into clinical trials database.</li><li>Serve as a resource for Clinical Trial Billing Information.</li><li>Coordinate protocol-specified procedures and treatments for study patients across disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and coordinate hands-on oncology nursing care.</li><li>Provide nursing assessment and documentation for study patients, ensuring accurate protocol adherence.</li><li>Collaborate with medical staff to ensure timely delivery of services to patients.</li><li>Grade adverse events and document toxicities as per protocol requirements.</li><li>Complete Serious/Unexpected Adverse Event (SAE) forms and ensure follow-up reports are accurate.</li><li>Assess overall protocol compliance and assist with deviation reporting.</li><li>Ensure bio-specimens are collected and processed according to protocol guidelines.</li><li>Assist with monitoring visits, audits, and sponsor queries.</li><li>Maintain research records for screened and enrolled patients.</li><li>Model professional responsibility and performance, and strive for professional growth.</li><li>Demonstrate competence in utilizing computerized systems required for clinical tasks.</li><li>Participate in training programs, quality assurance activities, and professional development.</li><li>Ensure adherence to Institutional, State, and Federal regulations and maintain mandatory educational requirements.</li></ul>Essential Skills<ul><li>Bachelor’s Degree in Nursing preferred.</li><li>License to practice nursing in the State of New Jersey.</li><li>One (1) year of oncology experience required.</li><li>Three (3) to five (5) 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 from the Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) as a Clinical Research Professional (CCRP) preferred.</li><li>Proficiency in computer applications such as Word, Excel, etc.</li><li>Excellent communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Detail-oriented with excellent organizational skills.</li><li>Experience and comfortability communicating with patients.</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 EnvironmentThe work environment involves being part of a statewide, national, and world leader of scientific discovery and patient care in cancer research. The role supports the conduct of innovative research and patient-centered care across various phases of trials, including adult and pediatric studies. The team operates at multiple sites with a focus on diverse disease-specific groups, with a goal of significant enrollment growth and trial activation.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 - $57.00/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 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Nurse Coordinator

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study.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 study conduct.</li><li>Perform nursing education to other disciplines for safe, effective care of enrolled patients.</li><li>Translate finalized protocol treatment plans into sample orders.</li><li>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.</li><li>Follow informed consent processes to ensure that IRB approved consent has been obtained and documented.</li><li>Provide backup support to register consented research patients and input data into clinical trials database.</li><li>Serve as a resource for Clinical Trial Billing Information.</li><li>Coordinate protocol-specified procedures and treatments for study patients across disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and coordinate hands-on oncology nursing care.</li><li>Provide nursing assessment and documentation for study patients, ensuring accurate protocol adherence.</li><li>Collaborate with medical staff to ensure timely delivery of services to patients.</li><li>Grade adverse events and document toxicities as per protocol requirements.</li><li>Complete Serious/Unexpected Adverse Event (SAE) forms and ensure follow-up reports are accurate.</li><li>Assess overall protocol compliance and assist with deviation reporting.</li><li>Ensure bio-specimens are collected and processed according to protocol guidelines.</li><li>Assist with monitoring visits, audits, and sponsor queries.</li><li>Maintain research records for screened and enrolled patients.</li><li>Model professional responsibility and performance, and strive for professional growth.</li><li>Demonstrate competence in utilizing computerized systems required for clinical tasks.</li><li>Participate in training programs, quality assurance activities, and professional development.</li><li>Ensure adherence to Institutional, State, and Federal regulations and maintain mandatory educational requirements.</li></ul>Essential Skills<ul><li>Bachelor’s Degree in Nursing preferred.</li><li>License to practice nursing in the State of New Jersey.</li><li>One (1) year of oncology experience required.</li><li>Three (3) to five (5) 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 from the Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) as a Clinical Research Professional (CCRP) preferred.</li><li>Proficiency in computer applications such as Word, Excel, etc.</li><li>Excellent communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Detail-oriented with excellent organizational skills.</li><li>Experience and comfortability communicating with patients.</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 EnvironmentThe work environment involves being part of a statewide, national, and world leader of scientific discovery and patient care in cancer research. The role supports the conduct of innovative research and patient-centered care across various phases of trials, including adult and pediatric studies. The team operates at multiple sites with a focus on diverse disease-specific groups, with a goal of significant enrollment growth and trial activation.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 - $57.00/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 5, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study.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 study conduct.</li><li>Perform nursing education to other disciplines for safe, effective care of enrolled patients.</li><li>Translate finalized protocol treatment plans into sample orders.</li><li>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.</li><li>Follow informed consent processes to ensure that IRB approved consent has been obtained and documented.</li><li>Provide backup support to register consented research patients and input data into clinical trials database.</li><li>Serve as a resource for Clinical Trial Billing Information.</li><li>Coordinate protocol-specified procedures and treatments for study patients across disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and coordinate hands-on oncology nursing care.</li><li>Provide nursing assessment and documentation for study patients, ensuring accurate protocol adherence.</li><li>Collaborate with medical staff to ensure timely delivery of services to patients.</li><li>Grade adverse events and document toxicities as per protocol requirements.</li><li>Complete Serious/Unexpected Adverse Event (SAE) forms and ensure follow-up reports are accurate.</li><li>Assess overall protocol compliance and assist with deviation reporting.</li><li>Ensure bio-specimens are collected and processed according to protocol guidelines.</li><li>Assist with monitoring visits, audits, and sponsor queries.</li><li>Maintain research records for screened and enrolled patients.</li><li>Model professional responsibility and performance, and strive for professional growth.</li><li>Demonstrate competence in utilizing computerized systems required for clinical tasks.</li><li>Participate in training programs, quality assurance activities, and professional development.</li><li>Ensure adherence to Institutional, State, and Federal regulations and maintain mandatory educational requirements.</li></ul>Essential Skills<ul><li>Bachelor’s Degree in Nursing preferred.</li><li>License to practice nursing in the State of New Jersey.</li><li>One (1) year of oncology experience required.</li><li>Three (3) to five (5) 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 from the Association of Clinical Research Professionals as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) as a Clinical Research Professional (CCRP) preferred.</li><li>Proficiency in computer applications such as Word, Excel, etc.</li><li>Excellent communication and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Detail-oriented with excellent organizational skills.</li><li>Experience and comfortability communicating with patients.</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 EnvironmentThe work environment involves being part of a statewide, national, and world leader of scientific discovery and patient care in cancer research. The role supports the conduct of innovative research and patient-centered care across various phases of trials, including adult and pediatric studies. The team operates at multiple sites with a focus on diverse disease-specific groups, with a goal of significant enrollment growth and trial activation.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 - $57.00/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 Feb 25, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study. The Clinical Research Nurse serves as a resource to 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 new clinical trial protocols.</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 protocol 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>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>Obtain informed consent for both therapeutic and non-therapeutic studies in accordance with IRB, GCP, and institutional policies.</li><li>Serve as a link between patients and all other members of the research team, addressing challenges with protocol completion and adherence.</li><li>Ensure protocol-specific orders are executed accurately, coordinating continuity of protocol-specified procedures between disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and deliver high-quality, compassionate oncology nursing care.</li><li>Collaborate with medical system staff to ensure coordinated and timely services for patients.</li><li>Grade adverse events using protocol-referenced NCI common toxicity criteria, provide informal teaching/coaching to clinicians, and complete SAE forms.</li><li>Assist in monitoring visits, audits, and providing responses to sponsor's queries.</li><li>Maintain research records for screened and enrolled patients, ensuring adherence to regulations and guidelines.</li></ul>Essential Skills<ul><li>Experience and comfortability communicating with patients.</li><li>Clinical research coordinator experience (1-3 years).</li><li>Proficiency in computerized systems (e.g., Word, Excel).</li><li>Excellent communication and interpersonal skills.</li><li>Detail-oriented with excellent organizational skills.</li><li>Ability to maximize resources and be resourceful.</li></ul>Additional Skills &amp; Qualifications<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; 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>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>Job Type &amp; LocationThis is a Contract to Hire position based out of Newark, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $55.00/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 Newark,NJ.Application DeadlineThis position is anticipated to close on Feb 25, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research NurseJob DescriptionThe primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective conduct of clinical trials. This role involves assisting investigators in preparing and implementing new clinical trials, screening and enrolling study participants, and providing protocol-related clinical management to those participants while on study. The Clinical Research Nurse serves as a resource to 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 new clinical trial protocols.</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 protocol 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>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>Obtain informed consent for both therapeutic and non-therapeutic studies in accordance with IRB, GCP, and institutional policies.</li><li>Serve as a link between patients and all other members of the research team, addressing challenges with protocol completion and adherence.</li><li>Ensure protocol-specific orders are executed accurately, coordinating continuity of protocol-specified procedures between disciplines/sites of care.</li><li>Manage patient reimbursement while on clinical trial and deliver high-quality, compassionate oncology nursing care.</li><li>Collaborate with medical system staff to ensure coordinated and timely services for patients.</li><li>Grade adverse events using protocol-referenced NCI common toxicity criteria, provide informal teaching/coaching to clinicians, and complete SAE forms.</li><li>Assist in monitoring visits, audits, and providing responses to sponsor's queries.</li><li>Maintain research records for screened and enrolled patients, ensuring adherence to regulations and guidelines.</li></ul>Essential Skills<ul><li>Experience and comfortability communicating with patients.</li><li>Clinical research coordinator experience (1-3 years).</li><li>Proficiency in computerized systems (e.g., Word, Excel).</li><li>Excellent communication and interpersonal skills.</li><li>Detail-oriented with excellent organizational skills.</li><li>Ability to maximize resources and be resourceful.</li></ul>Additional Skills &amp; Qualifications<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; 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>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>Job Type &amp; LocationThis is a Contract to Hire position based out of Newark, NJ.Pay and BenefitsThe pay range for this position is $55.00 - $55.00/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 Newark,NJ.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Research Nurse (Transplant)We are seeking a Clinical Research Nurse specializing in Transplant to join our dynamic team. This role is perfect for a motivated individual with a strong background in clinical research and nursing. You will coordinate and oversee the clinical operations of clinical trials, contributing to the assessment, planning, implementation, and evaluation of patient care in research studies.Responsibilities<ul><li>Assist the principal investigator in preparing proposed clinical trials by reviewing trial protocol and ensuring appropriate departments are notified.</li><li>Ensure all protocol revisions, informed consents, and serious adverse events are submitted to the appropriate IRB in a timely manner.</li><li>Act as a liaison between principal investigators and sub-investigators on regulatory issues.</li><li>Review studies for feasibility and evaluate potential competition with other protocols.</li><li>Recruit and evaluate study patients, schedule appointments, and conduct interviews.</li><li>Identify the needs of the patient population served and deliver care specific to those needs.</li><li>Review medical records for potential study patients and ensure comprehensive documentation.</li><li>Instruct study patients and healthcare providers on clinical trials, treatments, and side effects.</li><li>Assist in the consent process and ensure patients understand clinical trials.</li><li>Document study patients' medical histories and monitor their progress during trials.</li><li>Evaluate and develop study patient education materials.</li><li>Plan appropriate care for study patients under the direction of a physician or advanced practice nurse.</li><li>Report adverse events to the sponsor and IRB according to established timelines.</li><li>Coordinate research activities including scheduling laboratory tests and medical exams.</li><li>Perform and oversee clinical duties such as EKGs and blood serum processing.</li><li>Maintain accurate and up-to-date records for each patient in a clinical trial.</li><li>Prepare for sponsor monitor site visits and resolve any issues found.</li><li>Develop case report forms and assist in preparing for publication.</li><li>Provide education to all departments and attend research meetings and conferences.</li><li>Participate in staff meetings and in-service education.</li></ul>Essential Skills<ul><li>Graduate of an NLN/AACN accredited program in nursing.</li><li>3-5 years of clinical nursing experience.</li><li>Transplant RN experience required.</li><li>Adherence to the American Nurses Association standards.</li><li>Mandatory education on human subjects research.</li><li>NJ State Professional Registered Nurse License.</li></ul>Additional Skills &amp; Qualifications<ul><li>BSN preferred.</li><li>Experience with FDA regulatory, IND reporting, and Microsoft Office Suite.</li><li>Experience in clinical research, particularly in oncology or as a Clinical Research Coordinator.</li></ul>Work EnvironmentThis position offers flexible work hours, typically consisting of four 10-hour days from 7 AM to 6 PM. Employees can choose and coordinate start times with the team. The work environment is fast-paced, high-volume, and high-pressure, requiring efficiency and effectiveness. The team is diverse and supportive, providing a welcoming atmosphere for hardworking individuals. The role requires standing for a minimum of 6 hours a day, with occasional lifting, pushing, and pulling of at least 5 lbs.Job Type &amp; LocationThis is a Permanent position based out of Hackensack, NJ.Pay and BenefitsThe pay range for this position is $100000.00 - $120000.00/yr.Hackensack Meridian Healthcare perm benefits packageWorkplace TypeThis is a fully onsite position in Hackensack,NJ.Application DeadlineThis position is anticipated to close on Mar 4, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Research Nurse(Transplant)

Job Title: Clinical System LeaderJob DescriptionThe Clinical Systems Leader is responsible for implementing all related clinical systems actions used in the development of clinical trials within Early Clinical Development. The role requires collaboration with a cross-functional team of internal stakeholders and technology vendors to ensure the successful implementation and maintenance of technology solutions supporting clinical trials.Responsibilities<ul><li>Implement all related clinical systems such as Interactive Response Technologies (IxRS) and electronic Clinical Outcome Assessments (eCOA) actions for the ECD portfolio.</li><li>Closely manage study-related timelines and associated activities.</li><li>Lead the end-to-end specifications for the build of clinical systems for an assigned study or enterprise project, including requirements review, testing, deployment, maintenance, enhancement, and closeout.</li><li>Provide technical oversight to ensure clinical systems solutions adhere to the study protocol, industry regulations, best practices, and company policies, procedures, and guidelines.</li><li>Work independently with PET stakeholders and/or cross-functional project teams and collaboratively with the ECD IA team to share knowledge.</li><li>Proactively identify and track study-level technical issues to resolution, ensuring prompt resolution of system issues, document issues and risks, and implement mitigation plans in partnership with the study team and technology vendor project manager.</li><li>Communicate technical issues clearly, concisely, and professionally with internal and external stakeholders and departmental leadership.</li></ul>Essential Skills<ul><li>Bachelor's Degree in life science, computer science, engineering, information system, data science, or related discipline.</li><li>2-5 years of experience in Clinical Operations or Clinical Systems Management.</li><li>2-5 years of experience in IxRS/IRT and clinical-related systems.</li><li>Successful track record in leading the implementation of clinical systems such as IxRS/IRT, ePRO, and eCOA.</li><li>Working knowledge of Good Clinical Practices and FDA regulations governing clinical trial execution.</li><li>Excellent written and verbal communication skills and strong project management skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Familiar with documentation in a regulated environment.</li><li>Experience in Veeva is a plus.</li></ul>Work EnvironmentThis role follows a hybrid working model with three days in the office and two remote days. Anchor days are Tuesday through Thursday.Job Type &amp; LocationThis is a Contract position based out of South San Francisco, CA.Pay and BenefitsThe pay range for this position is $72.00 - $80.00/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 South San Francisco,CA.Application DeadlineThis position is anticipated to close on Feb 20, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical System Leader

We are seeking an experienced Clinical Team Lead to oversee and support country-level feasibility, investigator identification, and selection. This role involves managing the contracting process with investigational sites and local vendors, as well as overseeing the management of project allocated direct reports, including CRAs, Site Managers, and CTAs.Responsibilities<ul><li>Oversee and support the country-level feasibility and investigator identification and selection.</li><li>Manage the contracting process with investigational sites and local vendors.</li><li>Responsible for the overall management of the project, allocated direct reports, including CRAs, Site Managers, and CTAs.</li><li>Organize and facilitate internal project team meetings and ensure meeting minutes are reviewed, approved, and distributed.</li><li>Develop, review, and revise project documents such as Clinical Monitoring Plans and CRF completion guidelines.</li><li>Prepare the Site Management Plan for studies without a Lead Site Manager.</li><li>Support project managers in developing study-related SharePoint for document sharing and study status reporting.</li><li>Initiate corrective and preventative measures such as updating study guidance documents and performing quality assessments.</li><li>Support project managers in executing KPIs for assigned staff and site deliverables within time and budget constraints.</li><li>Review and verify documents for the first Investigational Medicinal Product release to investigational sites.</li><li>Support project managers in setting up and maintaining clinical trial master files and ensure quality control of assigned sections.</li><li>Review site visit reports and ensure they are finalized within expected timelines and quality standards.</li><li>Report unresolved site issues to project managers with action plans for discussion.</li><li>Review cumulative listings of study non-compliances and assess trends for corrective actions.</li><li>Inform project managers of any problems with investigators, sponsors, or partners, and escalate issues immediately.</li><li>Coordinate and ensure adequate preparations for site-specific audits and inspections, and analyze audit reports.</li></ul>Essential Skills<ul><li>Experience in clinical research and trial oversight.</li><li>Expertise in LATAM, trip report review, and oncology.</li><li>Knowledge of CRA KPIs, clinical trials, bid defense, and rare diseases.</li><li>Fluency in Spanish.</li></ul>Work EnvironmentThis is a fully remote position with the expectation of travel for bid defense meetings, possibly including international travel. You will have the opportunity to work on studies in both the US and EU, and transition to overseeing LATAM studies when awarded. Join a CRO gaining traction on new study awards.Job Type &amp; LocationThis is a Contract to Hire position based out of Parsippany-Troy Hills, NJ.Pay and BenefitsThe pay range for this position is $80.00 - $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 remote position.Application DeadlineThis position is anticipated to close on Feb 24, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Team Manager

Job Title: Clinical Trial ManagerJob DescriptionThe Clinical Trial Manager will oversee three new studies, including a self-administered Phase 3 study, a bioequivalence Phase 1 study, and a Pediatric Phase 3 study. This role involves coordinating operational aspects from study start-up through to the completion of the Clinical Study Report (CSR).Responsibilities<ul><li>Coordinate operational aspects of assigned studies from study start-up through CSR.</li><li>Generate, review, and maintain study project plans, including timeline, budget, and resources.</li><li>Manage comprehensive study timelines and metrics and oversee adherence.</li><li>Participate in management and oversight of vendors, performing ongoing reviews of vendor reports, budgets, and metrics.</li><li>Ensure vendor-related issues are promptly escalated, addressed, and brought to the attention of the management team.</li><li>Provide input and review of study-related clinical plans and documents such as CTA templates, Clinical Monitoring Plan, Patient Diary, and CRF Completion Guidelines.</li><li>Assist in the selection of sites and countries, assess operational feasibility, and facilitate start-up execution.</li></ul>Essential Skills<ul><li>Clinical trial management</li><li>Project management</li><li>Vendor management</li><li>Clinical study and bioequivalence study experience</li><li>Minimum 5 years of experience in Clinical Operations (e.g., CRA, Sr. CRA, CTM)</li><li>Minimum 3 years of experience in a clinical study management role as a CTM</li><li>Experience managing Dermatology clinical trials, particularly atopic dermatitis</li><li>Proven experience in oversight and management of CROs and other trial vendors</li><li>Strong project management skills, including budget, contract, and timeline management</li><li>Proven experience in early and late-stage clinical trials</li><li>Excellent communication, organizational, and problem-solving abilities</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a relevant field (Life Sciences, Nursing, or equivalent)</li><li>Ph.D. in a related life science discipline is preferred</li><li>Global experience</li><li>Experience managing drug-device combination product and self-administration clinical trials, preferred</li><li>Device experience is nice to have</li><li>Clinical research and clinical operation experience</li><li>Regulatory and site management experience</li></ul>Work EnvironmentThe role offers a long-term opportunity with great team support and learning opportunities. It is a highly visible position within the organization. Ideally, the individual can work in the Princeton office once a week. If not local, candidates on the East Coast are preferred.Job Type &amp; LocationThis is a Contract position based out of Princeton, NJ.Pay and BenefitsThe pay range for this position is $75.00 - $80.00/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 Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Clinical Trial Manager

Job Title: Clinical Trial ManagerJob DescriptionThe Clinical Trial Manager will oversee three new studies, including a self-administered Phase 3 study, a bioequivalence Phase 1 study, and a Pediatric Phase 3 study. This role involves coordinating operational aspects from study start-up through to the completion of the Clinical Study Report (CSR).Responsibilities<ul><li>Coordinate operational aspects of assigned studies from study start-up through CSR.</li><li>Generate, review, and maintain study project plans, including timeline, budget, and resources.</li><li>Manage comprehensive study timelines and metrics and oversee adherence.</li><li>Participate in management and oversight of vendors, performing ongoing reviews of vendor reports, budgets, and metrics.</li><li>Ensure vendor-related issues are promptly escalated, addressed, and brought to the attention of the management team.</li><li>Provide input and review of study-related clinical plans and documents such as CTA templates, Clinical Monitoring Plan, Patient Diary, and CRF Completion Guidelines.</li><li>Assist in the selection of sites and countries, assess operational feasibility, and facilitate start-up execution.</li></ul>Essential Skills<ul><li>Clinical trial management</li><li>Project management</li><li>Vendor management</li><li>Clinical study and bioequivalence study experience</li><li>Minimum 5 years of experience in Clinical Operations (e.g., CRA, Sr. CRA, CTM)</li><li>Minimum 3 years of experience in a clinical study management role as a CTM</li><li>Experience managing Dermatology clinical trials, particularly atopic dermatitis</li><li>Proven experience in oversight and management of CROs and other trial vendors</li><li>Strong project management skills, including budget, contract, and timeline management</li><li>Proven experience in early and late-stage clinical trials</li><li>Excellent communication, organizational, and problem-solving abilities</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a relevant field (Life Sciences, Nursing, or equivalent)</li><li>Ph.D. in a related life science discipline is preferred</li><li>Global experience</li><li>Experience managing drug-device combination product and self-administration clinical trials, preferred</li><li>Device experience is nice to have</li><li>Clinical research and clinical operation experience</li><li>Regulatory and site management experience</li></ul>Work EnvironmentThe role offers a long-term opportunity with great team support and learning opportunities. It is a highly visible position within the organization. Ideally, the individual can work in the Princeton office once a week. If not local, candidates on the East Coast are preferred.Job Type &amp; LocationThis is a Contract position based out of Philadelphia, PA.Pay and BenefitsThe pay range for this position is $75.00 - $80.00/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 Feb 27, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Clinical Trial ManagerJob DescriptionThe Clinical Trial Manager will oversee three new studies, including a self-administered Phase 3 study, a bioequivalence Phase 1 study, and a Pediatric Phase 3 study. This role involves coordinating operational aspects from study start-up through to the completion of the Clinical Study Report (CSR).Responsibilities<ul><li>Coordinate operational aspects of assigned studies from study start-up through CSR.</li><li>Generate, review, and maintain study project plans, including timeline, budget, and resources.</li><li>Manage comprehensive study timelines and metrics and oversee adherence.</li><li>Participate in management and oversight of vendors, performing ongoing reviews of vendor reports, budgets, and metrics.</li><li>Ensure vendor-related issues are promptly escalated, addressed, and brought to the attention of the management team.</li><li>Provide input and review of study-related clinical plans and documents such as CTA templates, Clinical Monitoring Plan, Patient Diary, and CRF Completion Guidelines.</li><li>Assist in the selection of sites and countries, assess operational feasibility, and facilitate start-up execution.</li></ul>Essential Skills<ul><li>Clinical trial management</li><li>Project management</li><li>Vendor management</li><li>Clinical study and bioequivalence study experience</li><li>Minimum 5 years of experience in Clinical Operations (e.g., CRA, Sr. CRA, CTM)</li><li>Minimum 3 years of experience in a clinical study management role as a CTM</li><li>Experience managing Dermatology clinical trials, particularly atopic dermatitis</li><li>Proven experience in oversight and management of CROs and other trial vendors</li><li>Strong project management skills, including budget, contract, and timeline management</li><li>Proven experience in early and late-stage clinical trials</li><li>Excellent communication, organizational, and problem-solving abilities</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor's degree in a relevant field (Life Sciences, Nursing, or equivalent)</li><li>Ph.D. in a related life science discipline is preferred</li><li>Global experience</li><li>Experience managing drug-device combination product and self-administration clinical trials, preferred</li><li>Device experience is nice to have</li><li>Clinical research and clinical operation experience</li><li>Regulatory and site management experience</li></ul>Work EnvironmentThe role offers a long-term opportunity with great team support and learning opportunities. It is a highly visible position within the organization. Ideally, the individual can work in the Princeton office once a week. If not local, candidates on the East Coast are preferred.Job Type &amp; LocationThis is a Contract position based out of Princeton, NJ.Pay and BenefitsThe pay range for this position is $75.00 - $80.00/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 Feb 26, 2026.<h2>About Actalent</h2>

 Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
 
 
 The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
 
 If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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