<h1 style="text-align: center;"><strong>Clinical Laboratory Technologist</strong></h1><p><br></p><h2>Job Description</h2><p>Join the Cell Kinetics Lab where you will be involved in testing for leukemia and lymphoma using blood, bone marrow, and tissue specimens. You&#39;ll work in an &#39;assembly line&#39; format where samples are processed through stages including pipetting, aliquotting, centrifuging, and chemical treatment to isolate white blood cells. These cells are then stained with antibodies and analyzed using flow cytometers. This dynamic role offers training across multiple benches, initially focusing on three key areas, with opportunities to expand into over ten other benches upon permanent employment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Perform pipetting, aliquotting, centrifuging, and chemical treatment of samples to isolate white blood cells.</li><li>Stain isolated white blood cells with antibodies.</li><li>Analyze stained cells using flow cytometers.</li><li>Train on multiple benches, with opportunities for further development upon permanent employment.</li></ul><h2>Essential Skills</h2><ul><li>Bachelor&#39;s degree in chemistry or a human biological science, including fields like Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Animal Science, Marine Biology, Neuroscience, etc.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with Flow cytometry or cell sorting is a plus.</li></ul>

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Clinical Laboratory Technologist - Mayo Clinic

<ul><li style="text-align: center;"><strong>Clinical Laboratory Technician (Entry-Level)</strong></li></ul><p><br></p><h2><u>Job Description:</u></h2><p>Perform analyses on blood, tissue, and body fluids to aid healthcare providers in the diagnosis, prognosis, and treatment of patients. Testing is conducted in specialized laboratories and may include highly skilled manual techniques or automated testing using sophisticated instrumentation.</p><p><br></p><h2><u>Responsibilities:</u></h2><ul><li>Operate and maintain laboratory instruments.</li><li>Troubleshoot assay systems and instruments.</li><li>Evaluate the accuracy of test results.</li><li>Assist in interpreting test results.</li><li>Provide operational support to optimize testing.</li><li>Work with multiple computer systems to retrieve and report information.</li><li>Adhere to safety protocols for handling infectious specimens, chemicals, and other hazards.</li><li>Assist with specimen collection as needed.</li></ul><h2><u>Additional Skills &amp; Qualifications:</u></h2><ol><li>Bachelor&#39;s degree in chemistry or a human biological science (e.g., Biology, Chemistry, Microbiology, Biochemistry, Molecular Biology, Animal Science, Marine Biology, Neuroscience).<ol><li>Chemistry and Biochemistry degrees preferred.</li></ol></li><li>Experience with instrumentation (GC, LC, HPLC, MS) preferred but not required.</li><li>Experience with laboratory practices in a college, research, or clinical setting is a plus but not required.</li><li>Master&#39;s degree accepted, but not PhD.</li></ol>

Clinical Mass Spectrometry Technician

<h1><strong>Job Title: Clinical Pharmacist</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Pharmacy Specialist is dedicated to contributing to the prevention and cure of cancer. This role involves providing safe, evidence-based, cost-effective, and patient-centered medication management as an integral part of the Malignant Hematology interdisciplinary team. The specialist will offer clinical pharmacy support to physicians, nurses, pharmacists, and other staff, both in hospital settings and ambulatory clinics. They will utilize their expertise to recommend, design, implement, monitor, and modify pharmaceutical care plans to optimize patient outcomes.</p><p><br></p><h2>Responsibilities</h2><ul><li>Provide oversight for 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.</li><li>Perform medication order review, clarification, and verification, ensuring completeness and appropriateness.</li><li>Supervise accurate preparation and distribution of hazardous and non-hazardous drugs per policies and procedures.</li><li>Process chemotherapy orders and conduct necessary double checks.</li><li>Develop, interpret, and provide medication-related information and education to 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>Lead the development, implementation, and maintenance of 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 cost-effective use of medications to ensure appropriate utilization of resources and reduce financial risk.</li></ul><h2>Essential Skills</h2><ul><li>Doctor of Pharmacy Degree</li><li>Board of Pharmacy Specialties (BPS) certification</li><li>Extensive clinical experience in disease state specialization</li><li>Pharmacy practice experience in medication safety and formulary management</li><li>Pathway/guideline and policy development/implementation</li><li>Oncology reimbursement and coverage</li><li>Clinical research involvement</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>PGY-2 Residency in Hematology/Oncology</li><li>Proficient in medical terminology</li><li>Experience with prior authorization processes</li><li>Strong <span style="color: rgb(8, 7, 7); background-color: none;">background</span> in health care and pharmaceutical care plans</li></ul><h2>Work Environment</h2><p>The work environment is supportive and collaborative, with a strong emphasis on teamwork and patient-centered care. Employees have access to professional development opportunities and appreciate the clean and safe environment maintained by the Environmental Services team. Efforts to maintain a good work-life balance are recognized, making it a fulfilling experience for those passionate about healthcare and patient support.</p>

Clinical Oncology Pharmacist

<h1><strong>Job Title: Clinical Oncology Pharmacist</strong></h1><p><br></p><p>This position is onsite in Tampa, FL. We are able to offer relocation assistance.</p><p><br></p><p><br></p><h2>Job Description</h2><p>The Clinical Pharmacy Specialist plays a crucial role in contributing to the prevention and cure of cancer. This position involves providing safe, evidence-based, and patient-centered medication management as part of the Malignant Hematology interdisciplinary team. The specialist offers clinical pharmacy support to various healthcare professionals, including physicians, nurses, and pharmacists, both in hospital settings and ambulatory clinics. The role demands a high level of expertise to recommend, design, implement, monitor, and modify pharmaceutical care plans to optimize patient outcomes. Additionally, the specialist actively participates in the education of patients, family members, healthcare providers, and pharmacy students and residents.</p><p><br></p><h2>Responsibilities</h2><ul><li>Provide oversight for safe and appropriate medication prescribing, dispensing, administering, and monitoring.</li><li>Optimize drug therapy for cancer patients through individualized treatment plans in collaboration with the healthcare team.</li><li>Perform medication order review, clarification, and verification, ensuring completeness and appropriateness.</li><li>Supervise accurate preparation and distribution of hazardous and non-hazardous drugs 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 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 in developing, implementing, and maintaining medication-related guidelines, policies, and standards.</li><li>Manage the medication use process to improve workflow, quality, and safety.</li><li>Ensure cost-effective use of medications to reduce financial risk.</li></ul><h2>Essential Skills</h2><ul><li>Doctor of Pharmacy Degree</li><li>Board of Pharmacy Specialties (BPS) certification</li><li>Extensive clinical experience in disease state specialization and pharmacy practice</li><li>Expertise in medication safety, formulary management, and policy development</li><li>Experience in oncology reimbursement and clinical research</li><li>Ability to educate patients, family members, and healthcare professionals</li><li>Competence in medication prescribing, dispensing, administering, and monitoring</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>PGY-2 Residency in Hematology/Oncology</li><li>Proficiency in medical terminology and prior authorization processes</li><li>Experience in compounding and hospital pharmacy settings</li></ul><h2>Work Environment</h2><p>The work environment is supportive and collaborative, with a strong focus on teamwork and patient-centered care. Professional growth is encouraged, and employees have access to various development opportunities. The environment is maintained as clean and safe, contributing to effective hospital operations. Efforts to maintain a good work-life balance are appreciated by staff. Overall, the work experience is fulfilling, especially for those passionate about healthcare and patient support.</p><p><br></p><p>Recruiter: Shelby Ciardelli</p>

Clinical Oncology Pharmacist - Relocation Offered

<h1 style="text-align: center;"><strong>Clinical Oncology Pharmacist - Tampa, FL</strong></h1><p><br></p><h2>Job Description</h2><ul><li>The Clinical Pharmacy Specialist is dedicated to the goal of contributing to the prevention and cure of cancer.</li><li>The Clinical Specialist provides safe, evidence-based, cost-effective, and patient-centered medication management as an integral part of the Malignant Hematology interdisciplinary team.</li><li>They are responsible for providing clinical pharmacy support to physicians, nurses, pharmacists, and other staff when caring for patients both in the hospital and ambulatory clinics.</li><li>The Clinical Specialist utilizes a high level of expertise to recommend, design, implement, monitor, and modify pharmaceutical care plans to optimize patient outcomes.</li><li>With extensive clinical experience within their disease state specialization, the Clinical Specialist contributes to medication safety, formulary management, pathway/guideline development, policy development/implementation, oncology reimbursement and coverage, and clinical research.</li><li>They also play an active role in the education of patients, family members, healthcare providers, and pharmacy students and residents.</li></ul><p><br></p><h2>Responsibilities</h2><ul><li>Provide oversight for 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 chemotherapy orders and perform necessary double checks.</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><h2>Essential Skills</h2><ul><li>Doctor of Pharmacy Degree</li><li>Board of Pharmacy Specialties (BPS) certification</li><li>Clinical pharmacist experience</li><li>Experience in medication prescribing, dispensing, administering, and monitoring</li><li>Chemotherapy order processing experience</li><li>Experience in medication therapy education and counseling</li><li>Experience in developing medication-related guidelines, policies, and standards</li><li>Experience with formulary management and pathway/guideline development</li><li>Knowledge of medication safety practices</li><li>Experience with oncology reimbursement and coverage</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>PGY-2 Residency in Hematology/Oncology</li><li>Experience in malignant hematology</li><li>Experience with interdisciplinary teams</li><li>Experience in clinical research</li><li>Experience in the education of patients and family members</li><li>Experience with policy development and implementation</li><li>Experience with prior authorization processes</li></ul>

Clinical Pharmacist

<h1 style="text-align: center;"><strong>Clinical Program Support Nurse (100% remote)</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Program Support Nurse will play a key role on our clinical program team, offering a unique blend of customer service and clinical expertise to beneficiaries enrolled in Medicare and Commercial plans. The nurse will engage in telephonic calls with plan beneficiaries, providers, pharmacists, and other stakeholders to discuss care gaps and potential solutions, driving outcomes for CMS Stars and HEDIS quality measures. Responsibilities include managing a caseload, analyzing data, and organizing and documenting all relevant interactions.</p><p><br></p><h2>Responsibilities</h2><ul><li>Responsible for member telephonic outreach to enhance medication therapy and drive strategic targeted initiatives forward.</li><li>Conduct clinical outreach to members, prescribers, and pharmacy providers to enhance care coordination.</li><li>Identify potential issues based upon information gathered during the interview with the member.</li><li>Recommend clinical case determinations on a case-by-case basis or escalate to clinical pharmacist for further evaluation.</li><li>Perform all necessary tasks in a platform with optimum quality and efficiency.</li><li>Ensure compliance with CMS guidelines for Medicare Stars programs and cost of care clinical programs.</li><li>Follow HIPAA, privacy, safety, and compliance guidelines.</li><li>Collaborate with team members to maintain clinical program services and exceed program expectations.</li><li>Stay updated on training levels, industry guidelines, literature, recommendations, and medications (prescription and OTC) to ensure program relevance and effectiveness.</li><li>Contribute to the development and implementation of innovative clinical outreach initiatives.</li><li>Follow all established health policies and procedures including but not limited to HIPAA, privacy and security policies and procedures.</li><li>Operate office equipment such as voice mail messaging systems, email, and use of various software applications to support operational processes.</li><li>Perform other duties or tasks, as assigned or required.</li></ul><h2>Essential Skills</h2><ul><li>Case management</li><li>Telephone customer service</li><li>Cardiology</li><li>Osteoporosis</li><li>Graduation from an accredited nursing program (LPN, RN) with an active license</li><li>Current nurse license in good standing with State Board of Nursing</li><li>1 year of relevant work experience in a clinical and/or managed care setting</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Ability to work as a team member, be professional and have telephonic communication skills.</li><li>Attention to detail and exercise professional work ethics.</li><li>Intermediate understanding of Microsoft Office Suite (Excel, Word, etc.) and knowledge of efficient record-keeping techniques.</li><li>Intermediate understanding and ability to navigate a database system.</li><li>Excellent written, verbal, and presentation skills with the ability to convey complex ideas to diverse audiences.</li><li>Strong analytical and problem-solving skills with attention to detail and quality.</li><li>Ability to work on multiple projects simultaneously under pressure with strict timelines.</li><li>Ability to develop process efficiencies.</li><li>Must have high-speed internet.</li><li>Experience with CMS Stars and HEDIS quality measures, risk revenue value streams, and population health management.</li><li>1 year of work experience in clinical, managed care and/or Pharmacy Benefit Management (PBM) setting.</li><li>Experience in health plan provider network performance management, population health management, continuous improvement or provider engagement models.</li><li>English: Required</li></ul><h2>Work Environment</h2><p>100% remote. The work schedule is Monday to Friday, 8:30 AM to 5:00 PM EST, with no weekends required. Continuous training is provided, starting with shadowing in the first week, followed by reverse shadowing in the second week, and ongoing monitoring and feedback from the third week onward.</p>

Clinical Program Support Nurse

<h1 style="text-align: center;"><strong>Job Title: Billing Manager </strong></h1><p><br></p><h2>Job Description</h2><p>The Manager of Research Billing Compliance is responsible for overseeing the development and execution of a research billing compliance program. This role is crucial in ensuring all legal and institutional requirements are met, while fostering a culture of compliance and ethical standards in research billing. The manager will lead a team, guiding them to achieve strategic and operational objectives while ensuring quality and productivity.</p><p><br></p><h2>Responsibilities</h2><ul><li>Manage daily work activities of the department staff to ensure quality, productivity, and functional excellence.</li><li>Assist in staffing decisions, including hiring and terminating employment.</li><li>Provide guidance and feedback to employees to help them strengthen specific knowledge and skills.</li><li>Facilitate effective team dynamics and teambuilding strategies.</li><li>Plan and organize day-to-day department operations and schedule activities.</li><li>Drive department service standards to impact customer satisfaction.</li><li>Ensure a safe and effective working environment, monitoring department safety plans and guidelines.</li><li>Respond to reported or suspected instances of research billing non-compliance.</li><li>Prepare policies and procedures associated with Clinical Research Billing Compliance.</li><li>Assist in budget development and manage department expenses within approved parameters.</li><li>Implement strategies to achieve financial targets and staffing needs.</li><li>Identify and implement innovative solutions for practice or workflow changes.</li></ul><h2>Essential Skills</h2><ul><li>Five years of progressively responsible experience related to research billing.</li><li>Proficiency in clinical research billing and EPIC.</li><li>Demonstrated skills and competencies necessary to perform the assigned job.</li><li>Effective communication skills across various channels.</li><li>Ability to interact confidently with patients, physicians, and co-workers.</li><li>Leadership qualities and critical thinking skills.</li><li>Strong analytical and interpersonal skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in business, hospital/healthcare administration, or a related field.</li><li>Master&#39;s degree preferred.</li><li>Ability to work effectively in a fast-paced environment.</li><li>Demonstrates flexibility and adaptability in the workplace.</li><li>Applies sound judgment in compliance and monitoring.</li></ul><h2>Work Environment</h2><p>This role offers an 8% bonus potential, which is rare for a clinical research role. The work environment is fast-paced and requires interaction with various healthcare professionals to ensure strong communication and seamless experiences. The role involves managing a small team and working with advanced systems like EPIC.</p>

Clinical Research Billing Manager

<p><strong>Position Summary:</strong></p><p>We are seeking a confident, assertive, and experienced Clinical Research Coordinator (CRC)to independently manage and execute clinical trials in a dynamic and fast-paced environment. The ideal candidate will have a strong experience in clinical research, with a preference for experience in allergy/immunology or dermatology. This role is ideal for a self-starter who thrives in an autonomous setting and is passionate about advancing clinical sciences. </p><p><br></p><p><strong>Key Responsibilities:</strong></p><ul><li>Independently coordinate and manage all aspects of clinical trials from initiation to close-out.</li><li>Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.</li><li>Serve as the primary point of contact for sponsors, monitors, and regulatory bodies.</li><li>Conduct subject recruitment, screening, informed consent, and study visits.</li><li>Collect, document, and maintain accurate study data and source documentation.</li><li>Manage investigational product accountability and coordinate lab sample processing and shipping.</li><li>Prepare for and participate in monitoring visits, audits, and inspections.</li><li>Maintain IATA certification and ensure proper handling and shipping of biological specimens.</li></ul><p><strong>Required:</strong></p><ul><li>Minimum 2 years of experience as a Clinical Research Coordinator.</li><li>Proven ability to work independently as the sole CRC on studies.</li><li>Confident and assertive communication style with strong organizational skills.</li><li>IATA certification (current and valid).</li><li>Associate’s degree with 3–5+ years of CRC experience, or Bachelor’s degree in a health-related field.</li></ul><p><strong>Preferred:</strong></p><ul><li>Experience in allergy/immunology or dermatology clinical trials.</li><li>Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).</li></ul>

Clinical Research Coordinator

<h1 style="font-weight: 700;">Job Title: Clinical Research Coordinator</h1><br><h2>Job Description</h2><p>As a Clinical Research Coordinator, you will oversee the day-to-day activities of clinical trials in accordance with Good Clinical Research Practice (GCP). You will interact with co-workers, visitors, and other staff in a manner that aligns with our values. Your role will involve training and supervising research staff on the proper procedures for conducting clinical trials per GCP, and you will be responsible for submitting all materials to the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol, ensuring compliance in a timely fashion.</p><br><h2>Responsibilities</h2><ul><li>Maintain accurate subject log and track expenses.</li><li>Submit appropriate documentation to Grant Administrator monthly for payment due for visits on all studies.</li><li>Perform regular quality control assessments to ensure clinical trial data collection and storage per GCP.</li><li>Organize and maintain documentation of all patient data.</li><li>Design electronic capture databases, if appropriate, and manage all collected data.</li><li>Provide clerical and technical support to ensure adherence to research protocols and quality of information received.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in clinical research practices.</li><li>Ability to conduct chart reviews and pre-screen patients.</li><li>Experience in cardiovascular research.</li><li>Knowledge of GCP and patient recruitment.</li><li>Familiarity with electronic data capture (EDC) systems.</li><li>Understanding of medical terminologies and procedures.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Minimum High School Diploma or equivalent.</li><li>Bachelor’s Degree or Master’s Degree preferred.</li><li>High School Diploma or equivalent with 6 years of clinical research experience and SOCRA certification required, OR Bachelor’s degree with 2 years of clinical research experience.</li><li>Experience in clinical research with a minimum of 1 year required.</li></ul><h2>Work Environment</h2><p>You will work in a combination of office and hospital/outpatient surgery settings. The environment is fast-paced with a high volume workload involving industry and investigator studies. This is a hybrid position requiring on-site presence about 3 days a week. The institute offers tuition reimbursement once permanent, excellent health benefits, opportunities for growth and upward mobility, and exposure to high-profile studies with renowned sponsors. You will gain great exposure to cardiovascular/device research within one of the world&#39;s most prestigious academic research institutes.</p><br>

<h1><strong>Clinical Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will manage multiple research trials, including first-in-human through phase 3 trials, ensuring compliance with FDA guidelines and adherence to Good Clinical Practice (GCP). This role involves daily interactions with clinicians, sponsors, IRB, regulatory agencies, and other research professionals. </p><p><br></p><h2>Responsibilities</h2><ul><li>Accurately prepare and maintain regulatory documents.</li><li>Prepare Informed Consent Documents with institutional language.</li><li>Interface with the IRB, preparing all required documents and submitting packages for review.</li><li>Collaborate with the recruitment team to create advertising plans and enroll subjects.</li><li>Monitor each subject’s schedule for compliance with the protocol.</li><li>Attend study meetings both internally and externally.</li><li>Train the study team on new and amended protocols.</li><li>Assist in operational planning for study visits, communicating needs to administration.</li><li>Create source documents to collect required data in RedCap and oversee team entries.</li><li>Assist in the execution of Informed Consent.</li><li>Enter data into study-specific databases.</li></ul><h2><strong>Required Skills &amp; Qualifications</strong></h2><ul><li>Clinical research coordination, screening, enrolling, and regulatory knowledge.</li><li>RedCap and various clinical databases proficiency.</li><li>Clinical Research certification by SOCRA or ACRP preferred.</li><li>Associates or Bachelor’s degree in a clinical or scientific field, or clinical certificate/license with</li><li>5+ years of clinical research experience required. </li><li>Cardiology experience preferred. </li></ul>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator serves as a vital resource for physician investigators and the scientific review committee regarding protocol specifics. This role involves interfacing with research sponsors and participating in on-site qualification and monitoring visits.</p><p><br></p><h2>Responsibilities</h2><ul><li>Act as a clinical research resource for protocol specifics to physician investigators and the scientific review committee.</li><li>Interface with research sponsors and participate in on-site qualification and monitoring visits.</li><li>Manage eCRFs and reporting, including addressing queries and handling adverse events (AEs) and serious adverse events (SAEs).</li><li>Direct and oversee daily activities of research protocols, including screening patients for protocol eligibility requirements.</li><li>Determine data requirements as specified by each individual research protocol.</li><li>Randomize patients appropriately and develop treatment plans according to specified protocols.</li><li>Collect appropriate data from physician offices and patient charts.</li><li>Ensure adequate documentation of all protocol-related parameters.</li></ul><h2>Essential Skills</h2><ul><li>Chart review experience.</li><li>Ability to pre-screen patients and recruit them for studies.</li><li>Skill in screening patient records in EMR to check eligibility for current and future research studies.</li><li>Experience supporting data entry or query resolution.</li></ul><h2>Work Environment</h2><p>The work environment consists of a small team where the coordinator will be the main point of contact for Cardiology studies currently open, with the potential for two additional studies coming soon.</p>

<h1 style="font-weight: 700;">Job Title: Clinical Research Coordinator</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Coordinator with over 2 years of experience in clinical research, specifically in supporting drug trials. This role involves patient interaction and meticulous data entry, with a focus on adverse event collection.</p><br><h2>Responsibilities</h2><ul><li>Coordinate and oversee clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines.</li><li>Conduct chart reviews and manage patient recruitment processes.</li><li>Pre-screen patients for clinical trials and manage regulatory documentation.</li><li>Enter and manage data using Electronic Data Capture (EDC) systems.</li><li>Collaborate with cross-functional teams in oncology to facilitate a variety of trials.</li></ul><h2>Essential Skills</h2><ul><li>Clinical research and trial management</li><li>Experience in chart review and patient recruitment</li><li>Knowledge of GCP and regulatory requirements</li><li>Proficiency in data entry and EDC systems</li><li>Experience in oncology and pre-screening patients</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree in a relevant field with 2+ years of clinical research experience</li><li>Experience in a healthcare setting</li><li>Successful completion of CITI Program and IATA training within 3 months of hire</li><li>Certification in research through a professional organization within 1 year of hire</li></ul><h2>Work Environment</h2><p>The role requires initial training on-site for 4-5 days a week, transitioning to 1 day of remote work per week for the first 6 months. Potential to increase remote work to 3 days per week based on performance and project needs. The work environment fosters growth and offers opportunities to participate in multiple oncology trials, providing a clear path to career advancement.</p><br>

<h1 style="text-align: center;"><strong>Clinical Research Coordinator</strong></h1><p><br></p><p>Clinical Research Coordinator (CRC) to coordinate day-to-day activities for clinical research studies across various therapeutic areas, including ophthalmology, dermatology, and pulmonology.</p><p>• Coordinate daily activities for clinical research studies across multiple therapeutic areas.</p><p>• Perform direct patient-facing duties, including informed consent, visit scheduling, and follow-up.</p><p>• Manage all aspects of patient recruitment and enrollment, including database reviews, outreach, pre-screening, and communications.</p><p>• Confidently perform blood draws and handle biospecimen processing and shipping according to protocol requirements.</p><p>• Maintain and manage study documentation, source data, and regulatory binders across various systems, including client&#39;s CTMS and sponsor EDC systems.</p><p>• Support monitoring visits and participate in both internal and external audits.</p><p>• Communicate effectively with sponsors, CROs, investigators, and internal departments.</p><p>• Provide general support to the team and step in across functions as needed to meet study goals.</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>2 years of Clinical Research experience</p><p>Bachelor’s degree</p><p>Phlebotomy</p><p>Certified Clinical Research Coordinator (CCRC) certification</p><p>Prior experience with multi-site clinical trials or decentralized trial models</p><p>Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms</p><p><span style="color: rgb(8, 7, 7); background-color: none;">Background</span> in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology</p><p>Fluent in Spanish (spoken and written)</p><p><br></p><p style="text-align: center;"><br></p>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><p><strong><u>Please Note: No Relocation Assistance Is Offered For This Position</u></strong></p><p><br></p><h2><strong>Job Description</strong></h2><p>The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This position involves a variety of tasks related to recruitment, data collection, data management, and reporting of results.</p><p><br></p><h2><strong>Responsibilities</strong></h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up with study participants through telephone, email, or 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></ul><h2><strong>Required Skills &amp; Experience</strong></h2><ul><li>High school diploma or General Education Development (GED).</li><li>6-12 months of clinical research experience.</li><li>Experience with chart review, patient recruitment, and clinical research.</li><li>Knowledge of EDC, EMR, and GCP.</li><li>Pre-screening patients.</li></ul><h2><strong>Additional Skills &amp; Qualifications</strong></h2><ul><li>Phlebotomy experience is a plus.</li></ul>

<h1 style="font-weight: 700;">Job Title: Clinical Research Coordinator</h1><br><h2>Job Description</h2><p>Join a prestigious academic research institute renowned for its state-of-the-art equipment and high-profile studies. This role involves working with large, well-known sponsors to advance cancer research.</p><br><h2>Responsibilities</h2><ul><li>Coordinate and manage clinical research projects, ensuring compliance with research protocols.</li><li>Interact comfortably with physicians and other healthcare professionals.</li><li>Manage patient enrollment, informed consent, chart reviews, and scheduling.</li><li>Perform data entry and utilize electronic data capture (EDC) systems.</li><li>Support oncology and hematology research, focusing on cancer medications and adverse event reporting using CTCAE 4.0.</li><li>Ensure compliance with IRB and human research protection regulations.</li><li>Work collaboratively within a team and independently to achieve research goals.</li></ul><h2>Essential Skills</h2><ul><li>Minimum of two to three years of clinical research experience.</li><li>Experience in oncology and hematology, with a preference for experience with cancer medications.</li><li>Effective communication and writing skills.</li><li>Ability to multi-task and problem-solve efficiently.</li><li>Strong proficiency in MS Office Suite and computer skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with IRB and human research protection regulations.</li><li>Hematology experience preferred.</li><li>Strong ability to work both independently and as part of a team.</li></ul><h2>Work Environment</h2><p>The work environment is fast-paced and located on a large campus. You will be part of the largest lymphoma team in the cancer center, consisting of 2 Project Managers, a Nurse Practitioner, 5 Clinical Research Nurses, 5 Clinical Research Coordinators, and 3 Research Assistants. The team aligns with specific Principal Investigators to support a bulk of work focused on CAR-T studies. The Cancer Center enjoys a vibrant, well-funded research base with a focus on reducing cancer incidence, mortality, and morbidity, while training future cancer researchers. The center holds over $145 million in grant funding and ranks highly in funding from the National Cancer Institute and American Cancer Society. Research excellence includes translational research, breast cancer, melanoma, hematologic malignancies, innovative clinical trials, tobacco research, developmental therapeutics, and immunobiology.</p><br>

<h1><strong>Clinical Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will manage multiple research trials, including first-in-human through phase 3 trials, ensuring compliance with FDA guidelines and adherence to Good Clinical Practice (GCP). This role involves daily interactions with clinicians, sponsors, IRB, regulatory agencies, and other research professionals. </p><p><br></p><h2>Responsibilities</h2><ul><li>Accurately prepare and maintain regulatory documents.</li><li>Prepare Informed Consent Documents with institutional language.</li><li>Interface with the IRB, preparing all required documents and submitting packages for review.</li><li>Collaborate with the recruitment team to create advertising plans and enroll subjects.</li><li>Monitor each subject’s schedule for compliance with the protocol.</li><li>Attend study meetings both internally and externally.</li><li>Train the study team on new and amended protocols.</li><li>Assist in operational planning for study visits, communicating needs to administration.</li><li>Create source documents to collect required data in RedCap and oversee team entries.</li><li>Assist in the execution of Informed Consent.</li><li>Enter data into study-specific databases.</li></ul><h2><strong>Required Skills &amp; Qualifications</strong></h2><ul><li>Clinical research coordination, screening, enrolling, and regulatory knowledge.</li><li>RedCap and various clinical databases proficiency.</li><li>Clinical Research certification by SOCRA or ACRP preferred.</li><li>Associates or Bachelor’s degree in a clinical or scientific field, or clinical certificate/license with</li><li>3+ years of clinical research experience required.</li><li>Cardiology experience preferred.</li></ul>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><p>This is an onsite contract position, contract is currently scoped for 4 months with potential for extension. </p><p><br></p><h2>Job Description</h2><p>We are seeking a skilled Clinical Research Coordinator with experience in clinical research to assist a research site with an pneumococcal vaccine study. This is a contract position lasting approximately four months, requiring a commitment of 24 hours per week.</p><p><br></p><h2>Responsibilities</h2><ul><li>Community &amp; Physician outreach</li><li>Recruitment through chart review &amp; phone screening</li><li>Appointment scheduling and reminders</li><li>Medical record retrieval</li></ul><h2>Essential Skills</h2><ul><li>Experience in clinical research</li><li>Proficient in using EMR systems</li><li>Prior experience as a Clinical Research Coordinator, ideally 2+ years</li><li>Bilingual in Spanish, not required but preferred</li></ul><p>Recruiter: Shelby Ciardelli</p>

<h1><strong>Job Title: Clinical Research Coordinator</strong></h1><p><br></p><h2>Job Description</h2><p>The Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This position involves a variety of tasks related to recruitment, data collection, data management, and reporting of results.</p><p><br></p><h2>Responsibilities</h2><ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including screening for eligibility.</li><li>Perform follow-up with study participants through telephone, email, or 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></ul><h2>Required Skills &amp; Experience</h2><ul><li>High school diploma or General Education Development (GED).</li><li>6-12 months of clinical research coordinator experience.</li><li>Experience with chart review, patient recruitment, and clinical research.</li><li>Knowledge of EDC, EMR, and GCP.</li><li>Pre-screening patients.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Phlebotomy experience is a plus.</li></ul><h2>Work Environment</h2><p>This position requires working onsite for 5 days a week, totaling 40 hours. You will have the opportunity to work in clinical research trials and support one of the leading healthcare providers in the US. The role offers opportunities for advancement, including roles such as CRC II, Team Lead, and Project Manager.</p>

<h1 style="font-weight: 700;">Job Title: Clinical Research Coordinator</h1><br><h2>Job Description</h2><p>We are seeking a dedicated Clinical Research Coordinator to join our prestigious academic research institute. This role involves recruiting, screening, and enrolling subjects into clinical trials, explaining the informed consent process, documenting adverse events, and collecting essential study documents. The coordinator will also be responsible for preparing Institutional Review Board applications, supporting CAR-T sponsor drug trials, and being part of starting up new studies.</p><br><h2>Responsibilities</h2><ul><li>Recruit, screen, and enroll subjects into clinical trials.</li><li>Explain the informed consent process to participants.</li><li>Document adverse events as they occur during trials.</li><li>Collect study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.</li><li>Prepare Institutional Review Board (IRB) applications.</li></ul><h2>Essential Skills</h2><ul><li>Enrollment and informed consent process knowledge.</li><li>Experience in patient oncology research.</li><li>Proficiency in clinical research coordination and data entry.</li><li>Ability to conduct chart reviews and understand regulatory requirements.</li><li>Experience in patient recruitment and consenting.</li><li>Effective communication and writing skills.</li><li>Knowledge of IRB and human research protection regulations.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor&#39;s degree (BA/BS) preferred.</li><li>1-3 years of clinical research experience required.</li><li>Experience with in-hospital clinical research.</li><li>Experience with adverse event reporting.</li></ul><h2>Work Environment</h2><p>The role involves working in a combination of office and hospital/outpatient surgery settings, within a very fast-paced and high-volume workload environment. You will be part of the largest team at the cancer center, with ample support, working on high-profile studies with large, well-known sponsors. The institute is equipped with state-of-the-art facilities, and the position offers the opportunity to work on industry-leading and investigator studies.</p><br>

Clinical Research Coordinator (On Site/Hybrid)

<p><strong>Description</strong></p><p>Overview:</p><p>We are seeking a driven and adaptable Clinical Research Coordinator I (CRC I) to support clinical trials across multiple locations. This is an entry-level role designed for candidates with a hands-on medical <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;">background</span></span> and strong patient interaction experience, such as medical assistants, phlebotomists, EMTs, or similar roles. As a CRC I, you will be part of a growing clinical operations team, gaining direct experience in the coordination of clinical trials. This position offers hands-on learning, mentorship, and full support in developing your clinical research skills.</p><p><br></p><p>Key Responsibilities include (but are not limited to):</p><p>• Assist in executing clinical trial activities under the guidance of experienced team members</p><p>• Support patient-facing responsibilities including scheduling, check-ins, and follow-up communication</p><p>• Participate in subject screening, enrollment, and retention efforts</p><p>• Enter and maintain accurate study data, and assist with resolving queries in electronic data capture (EDC) systems</p><p>• Attend site initiation visits and investigator meetings as needed</p><p>• Prepare and organize study documentation, source materials, and regulatory files</p><p>• Coordinate appointment scheduling and assist in ensuring visit compliance</p><p>• Communicate with site staff, patients, and sponsor or CRO representatives</p><p>• Travel between locations and satellite sites as needed</p><p><br></p><p><strong>Additional Skills &amp; Qualifications</strong></p><p>Required Qualifications:</p><p>• Prior medical or clinical experience in a patient-facing role (e.g., MA, phlebotomist, EMT, CNA, LPN, etc.)</p><p>• Strong interpersonal and organizational skills</p><p>• Basic familiarity with medical terminology or healthcare procedures</p><p>• Comfort with technology and ability to learn EDC systems</p><p>• Ability to multitask in a dynamic, detail-oriented environment</p><p>• Willingness to travel to support multiple study sites</p><p><br></p><p>Preferred Qualifications:</p><p>• Fluent in Spanish (spoken and written)</p><p>• Familiarity with clinical trial management systems (CTMS) and electronic regulatory platforms</p><p>• <span style="background-color: none; color: rgb(8, 7, 7);"><span style="color: rgb(8, 7, 7); background-color: none;">Background</span></span> in therapeutic areas such as Ophthalmology, Dermatology, or Pulmonology</p>

Clinical Research Coordinator I

<h1><strong><em>﻿</em>Clinical Research Coordinator II </strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator (Non-RN) plays a pivotal role in managing research studies, trials, and programs. This includes patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers participating in research. The coordinator is responsible for recruiting and consenting research participants, providing exceptional patient-facing interactions, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure compliance with regulations and protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute and coordinate the informed consent process for participants in clinical trials and research studies across various locations, which may involve travel or the use of technology.</li><li>Oversee all aspects of research, including patient screening, eligibility assessment, and volunteer participation and follow-up.</li><li>Coordinate the recruitment and consenting of research participants for therapeutic areas served.</li><li>Deliver concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to biospecimens used in research; conduct patient chart review 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/data mining into registries, patient records, and research-specific database systems.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and 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 standard operating procedures (SOP) for the research division, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing project budgets from internal and external funding sources.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work independently in a fast-paced clinical or research environment, managing multiple tasks efficiently and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar ethical treatment awareness in research.</li><li>Effective communication with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem solving, fact analysis, and sound judgment application.</li><li>Ability to accept direction and adapt to the evolving needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field (no experience required).</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><p style="text-align: center;"><strong>Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for next steps information.</strong></p><h2><br></h2>

Clinical Research Coordinator II

<h1><strong>Clinical Research Coordinator II </strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator (Non-RN) plays a pivotal role in managing research studies, trials, and programs. This includes patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers participating in research. The coordinator is responsible for recruiting and consenting research participants, providing exceptional patient-facing interactions, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure compliance with regulations and protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute and coordinate the informed consent process for participants in clinical trials and research studies across various locations, which may involve travel or the use of technology.</li><li>Oversee all aspects of research, including patient screening, eligibility assessment, and volunteer participation and follow-up.</li><li>Coordinate the recruitment and consenting of research participants for therapeutic areas served.</li><li>Deliver concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to biospecimens used in research; conduct patient chart review 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/data mining into registries, patient records, and research-specific database systems.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and 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 standard operating procedures (SOP) for the research division, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing project budgets from internal and external funding sources.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work independently in a fast-paced clinical or research environment, managing multiple tasks efficiently and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar ethical treatment awareness in research.</li><li>Effective communication with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem solving, fact analysis, and sound judgment application.</li><li>Ability to accept direction and adapt to the evolving needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field (no experience required).</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><h2><br></h2>

<h1><strong><em>﻿</em>Clinical Research Coordinator II </strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator (Non-RN) plays a pivotal role in managing research studies, trials, and programs. This includes patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers participating in research. The coordinator is responsible for recruiting and consenting research participants, providing exceptional patient-facing interactions, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure compliance with regulations and protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute and coordinate the informed consent process for participants in clinical trials and research studies across various locations, which may involve travel or the use of technology.</li><li>Oversee all aspects of research, including patient screening, eligibility assessment, and volunteer participation and follow-up.</li><li>Coordinate the recruitment and consenting of research participants for therapeutic areas served.</li><li>Deliver concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to biospecimens used in research; conduct patient chart review 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/data mining into registries, patient records, and research-specific database systems.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and 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 standard operating procedures (SOP) for the research division, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing project budgets from internal and external funding sources.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work independently in a fast-paced clinical or research environment, managing multiple tasks efficiently and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar ethical treatment awareness in research.</li><li>Effective communication with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem solving, fact analysis, and sound judgment application.</li><li>Ability to accept direction and adapt to the evolving needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet skills.</li></ul>

<h1><strong><em>﻿</em>Clinical Research Coordinator II </strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Coordinator (Non-RN) plays a pivotal role in managing research studies, trials, and programs. This includes patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers participating in research. The coordinator is responsible for recruiting and consenting research participants, providing exceptional patient-facing interactions, and coordinating biospecimen collection through collaboration with clinical research nursing staff, laboratory teams, and hospital departments to ensure compliance with regulations and protocols.</p><p><br></p><h2>Responsibilities</h2><ul><li>Execute and coordinate the informed consent process for participants in clinical trials and research studies across various locations, which may involve travel or the use of technology.</li><li>Oversee all aspects of research, including patient screening, eligibility assessment, and volunteer participation and follow-up.</li><li>Coordinate the recruitment and consenting of research participants for therapeutic areas served.</li><li>Deliver concierge-level service for all patient-facing interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain a HIPAA-protected database linking patient information to biospecimens used in research; conduct patient chart review 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/data mining into registries, patient records, and research-specific database systems.</li><li>Assist Principal Investigators and research staff in developing compliant research protocols and 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 standard operating procedures (SOP) for the research division, ensuring compliance with clinical research standards and procedures.</li><li>Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing project budgets from internal and external funding sources.</li></ul><h2>Essential Skills</h2><ul><li>Ability to work independently in a fast-paced clinical or research environment, managing multiple tasks efficiently and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar ethical treatment awareness in research.</li><li>Effective communication with research participants, investigators, research staff, and external partners.</li><li>Analytical approach to problem solving, fact analysis, and sound judgment application.</li><li>Ability to accept direction and adapt to the evolving needs of clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet skills.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field (no experience required).</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><p style="text-align: center;"><br></p><h2><br></h2>

Clinical Research Coordinator II (TRI)

<h1><strong>Clinical Research Data Supervisor</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Data Operations Supervisor is pivotal in ensuring a safe, secure, and healthy work environment. This role involves leading the hiring process, developing the team through one-on-one discussions, and managing the performance of research team members. You will collaborate with Clinical Research Supervisors to oversee the daily activities of the clinical research team, ensuring productivity and effective personnel scheduling. As an expert resource, you will address any barriers during operations and monitor the quality of data operations.</p><p><br></p><h2>Responsibilities</h2><ul><li>Ensure a safe, secure, and healthy work environment.</li><li>Lead the hiring process, including applicant review and selection.</li><li>Facilitate team development through one-on-one discussions.</li><li>Manage performance of research team members, providing feedback and conducting Talent Care discussions.</li><li>Collaborate with Clinical Research Supervisors to oversee daily activities of the research team.</li><li>Supervise team workflow productivity and maintain staffing schedules.</li><li>Serve as an expert resource for the research team.</li><li>Monitor and evaluate data operations quality, reviewing monitor follow-up visit letters and sponsor reports.</li></ul><h2>Essential Skills</h2><ul><li>Data management</li><li>Oncology</li><li>Clinical research</li><li>Clinical research data</li><li>Supervision</li><li>EDC (Electronic Data Capture)</li><li>Data collection</li><li>Data review</li><li>Bachelor’s Degree in Healthcare Administration, Research, or related field with at least 2 years of clinical research experience</li><li>Associate’s Degree in Healthcare Administration, Research, or related field with at least 3 years of clinical research experience</li><li>Preferred: Master’s degree in Healthcare Administration, Research, or related field</li><li>Preferred: 5 years of clinical research experience with increasing management responsibilities</li><li>Advanced training/experience in data-related items, databases, and various EDC systems</li></ul><h2>Work Environment</h2><p>The role primarily involves working onsite, with occasional travel to other locations as necessary.</p>

Clinical Research Data Supervisor

<h1><strong>Clinical Research Laboratory Assistant</strong></h1><p><br></p><h2>Job Description</h2><p>Join our dynamic team as a Clinical Research Laboratory Assistant, where you will work in a laboratory setting to process blood samples according to research protocols. You will be responsible for processing, storing, and shipping samples, ensuring adherence to specific temperature and labeling requirements. This role does not involve direct patient interaction and offers a fast-paced work environment.</p><p><br></p><h2>Responsibilities</h2><ul><li>Process blood samples according to research protocol.</li><li>Store and ship samples per protocol, ensuring specific temperature and labeling requirements are met.</li><li>Collaborate in a fast-paced lab environment with other Clinical Research Assistants.</li><li>Maintain organization to ensure timely processing of samples according to protocols.</li></ul><h2>Required Skills &amp; Experience</h2><ul><li>Experience in laboratory or healthcare sample processing (1-2 years required).</li><li>Proficiency in specimen processing and labeling.</li><li>High School Diploma.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Research experience is a plus.</li><li>Experience in clinical trials is advantageous.</li><li>Oncology experience is beneficial.</li></ul>

Clinical Research Laboratory Assistant

<h1><strong>Job Title: Clinical Research Nurse</strong></h1><p><br></p><h2>Job Description</h2><p>The Clinical Research Nurse will play a pivotal role in supporting clinical trials by performing routine operational activities for multiple research protocols. </p><p><br></p><h2>Responsibilities</h2><ul><li>Complete all training assignments by the specified due dates.</li><li>Perform routine operational activities for multiple research protocols.</li><li>Liaise between site research personnel, industry sponsors, and work closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable.</li><li>Coordinate schedule of assessments from initial submission of feasibility until study closeout.</li><li>Review study design and inclusion/exclusion criteria with physician and patient.</li><li>Ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements.</li><li>Ensure the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitor data for missing or implausible data.</li><li>Create study-specific tools for source documentation when not provided by sponsor.</li><li>Collect, complete, and enter data into study-specific case report forms or electronic data capture systems.</li><li>Generate and track drug shipments, device shipments, and supplies as needed.</li><li>Ensure timely and accurate data completion.</li></ul><h2>Required Skills &amp; Experience</h2><ul><li>Clinical research experience.</li><li>Active RN license. </li><li>One year of oncology experience or three years of experience in other indications.</li></ul><h2><br></h2>

Clinical Research Nurse

<h1 style="font-weight: 700;">Job Title: Clinical Research Nurse</h1><br><h2>Job Description</h2><p>The Clinical Research Coordinator II RN (CRC-II RN) plays a pivotal role in the research institute, operating under limited supervision to plan, coordinate, evaluate, and perform nursing care for participants, while collecting data for assigned research projects. This role adheres to study-specific protocol guidelines and communicates effectively with Principal Investigators, Sub-Investigators, Clinical Research Leads, and research support staff. The CRC-II RN advocates for patient care while ensuring compliance with industry-sponsored and investigator-initiated clinical trials, following FDA regulations and ICH/GCP guidelines.</p><br><h2>Responsibilities</h2><ul><li>Deliver safe care and demonstrate regard for the dignity and respect of all participants.</li><li>Maintain clinical competencies including physical assessment, phlebotomy, and IV insertion.</li><li>Practice the principles of Universal Precautions and abide by HIPAA regulations.</li><li>Maintain a clean and prepared clinical space, performing set-up and turnover procedures according to SOPs.</li><li>Participate in training programs to maintain licensure.</li><li>Utilize positive interpersonal communication skills with healthcare team, patients, investigators, sponsors, and administration.</li><li>Review informed consent documents according to regulations with study candidates or their legal representatives.</li><li>Manage multiple clinical trial protocols, coordinate execution and follow-up, and perform accurate documentation.</li><li>Promote Principal Investigator oversight by advising of deviations in conduct and patient status.</li><li>Coordinate work of support staff, laboratory technicians, and assistants for efficient and high-quality results.</li><li>Serve as liaison between Principal Investigators and the Institutional Review Board and Office of Sponsored Programs.</li><li>Prepare and review documentation for clinical research study startup, execution, modification, renewal, and termination.</li><li>Remain current on regulatory requirements and HIPAA regulations, implementing changes as needed.</li></ul><h2>Essential Skills</h2><ul><li>Clinical research expertise</li><li>Knowledge of Good Clinical Practice (GCP)</li><li>Pre-screening patients</li><li>Registered Nurse qualifications</li><li>IV infusion skills</li><li>Electronic Data Capture (EDC)</li><li>Chart review proficiency</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Associate degree in Nursing</li><li>Minimum 2 years of Clinical Research experience</li><li>Current active State of Florida license as a Registered Nurse</li><li>Basic Life Support (BLS) certification</li></ul><h2>Work Environment</h2><p>This position is based in a hospital setting, requiring adherence to clinical protocols and maintaining professionalism in a dynamic healthcare environment.</p><br>

<p style="text-align: center;"><strong><u>Clinical Research Nurse</u></strong></p><p style="text-align: center;"><em>Must be able to commute to</em></p><p style="text-align: center;"><em>Phildelphia, PA</em></p><p style="text-align: center;"><br></p><p style="text-align: center;"><br></p><p><strong>Responsibilities</strong></p><p>The Clinical Research Nurse performs basic nursing skills, study coordination and data management, with a central focus on managing subject recruitment and</p><p>enrollment, consistency of study implementation, data management and integrity ,and compliance with regulatory requirements and reporting.</p><ul><li>Collects and documents clinical information (data) from study participants.</li><li>Provides patient education regarding research study.</li><li>Obtains informed consent and supports enrollment into clinical trials.</li><li>Interacts with consortium members, organizes meetings and communicates with participating institutions, tracks and records progress, schedules meetings, records and distributes minutes.</li></ul><p><strong>Qualifications</strong></p><p>Pennsylvania Registered Nursing License</p><p>2+ years of experience within a hospital setting </p><p>Bachelors Degree </p><p>Oncology experience preferred</p><p>Interest in exploring the clinical research field </p>

Clinical Research Nurse - Oncology

<p><strong><u>Clinical Research Nurse Coordinator</u></strong></p><p>Coordinate and perform nursing care for clinical trial participants under limited supervision</p><p>Ensure compliance with FDA regulations and ICH/GCP guidelines</p><p>Collaborate with Principal Investigators, Sub-Investigators, and research staff</p><p>Serve as a liaison with the IRB and Office of Sponsored Programs</p><p>Support  research, with a focus on IV infusion and trial execution</p><p>Perform IV Infusions  </p><p>Phlebotomy </p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>Associate degree in Nursing and current RN license</p><p>ACLS certification</p><p>Minimum 2 years of clinical research experience</p><p>Strong IV and infusion skills</p><p>Phlebotomy </p><p><br></p>

Clinical Research Nurse Coordinator

<p><strong><u>Clinical Research Nurse Coordinator</u></strong></p><p>Coordinate and perform nursing care for clinical trial participants under limited supervision</p><p>Ensure compliance with FDA regulations and ICH/GCP guidelines</p><p>Collaborate with Principal Investigators, Sub-Investigators, and research staff</p><p>Serve as a liaison with the IRB and Office of Sponsored Programs</p><p>Support Surgery and Digestive Health research, with a focus on IV infusion and trial execution</p><p><br></p><p><strong><u>Qualifications</u></strong></p><p>Associate degree in Nursing and current RN license</p><p>ACLS certification</p><p>Minimum 2 years of clinical research experience</p><p>Strong IV and infusion skills</p><p>Flexibility to support early OR procedures (approx. once a week)</p><p>ALSO open to Infusion RN with 4–6 years of experience, eager to transition into research</p><p><br></p><p><strong><u>Schedule</u></strong></p><p>Monday–Friday, 8:00 AM–4:30 PM, with flexibility for early OR starts (typically 5:45 AM). Adjusted hours and early leave options are available based on weekly schedules</p><p><br></p>

Clinical Research Nurse II

<p style="text-align: center;"><strong>Clinical Research Nurse Practitioner- Sub Investigator</strong></p><p style="text-align: center;"><br></p><p><strong><u>Key Responsibilities</u></strong></p><p>•	Serve as the Sub Investigator and conduct study activities as delegated by the Principal Investigator and Study Project Manager, in compliance with study   protocols and applicable FDA regulations.</p><p>•	Perform vital signs assessments, physical examinations, phlebotomy, and other clinical procedures as required by trial protocols.</p><p>•	Order diagnostic tests and liaise with clinical departments and specialists according to the trial schedule.</p><p>•	Oversee study drug dispensation, preparation, administration, and maintain accurate study drug logs and documentation.</p><p>•	Monitor and record patient responses to treatment, adverse events (AEs), and serious adverse events (SAEs).</p><p>•	Coordinate medical procedures and patient treatment plans with investigators and the Medical Director.</p><p>•	Ensure precise and timely documentation, including completion of Case Report Forms (CRFs) and maintenance of source documentation.</p><p>•	Prescribe medications and treatments as necessary and obtain informed consent from trial participants in accordance with ICH GCP and Arensia SOPs.</p><p>•	Handle medical emergencies in accordance with study protocols and applicable regulations.</p><p>•	Assist with study feasibility reviews and provide medical and scientific feedback on trial protocols and study records.</p><p>•	Collaborate with study coordinators to ensure proper trial setup and adequate inventory of investigational products and study supplies.</p><p>•	Participate in patient recruitment, screening, and retention efforts.</p><p>•	Contribute to the development and review of internal documentation, including SOPs and templates.</p><p>•	Participate in monitoring visits, audits, and inspections by sponsors and related agencies to ensure data accuracy and quality.</p><p>•	Perform other duties as assigned.</p><p><strong><u>Qualifications</u></strong></p><p>•	Master’s degree in Nursing (MSN) from an accredited institution with advanced clinical training.</p><p>•	Minimum of one year of experience as a nurse practitioner.</p><p>•	Active and unencumbered license to practice as a registered nurse in Arizona.</p><p>•	National NP Certification.</p><p>•	Experience with clinical research principles and procedures.</p><p>•	Familiarity with instruments and equipment commonly used in clinical research.</p><p>•	Understanding of ethical principles and federal and state regulations governing human subjects in clinical research.</p><p>•	Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures.</p><p>•	CPR/ACLS certification, GCP, and IATA training (initial certifications and recertifications supported by ARENSIA).</p><p>•	Proficiency in the Spanish language is advantageous.</p><p><br></p><h2><br></h2>

Clinical Research Nurse Practitioner-Sub I

<h1 style="text-align: center;"><strong>Actalent is hiring UM nurses!</strong></h1><h2>Job Description</h2><p>The Utilization Management Nurse (UMN) plays a crucial role in optimizing the utilization of healthcare services. Working under the general supervision of the Director and/or Manager/Supervisor of Medical Management, and in collaboration with an interdisciplinary team, the UMN reviews service authorization requests to ensure appropriate service utilization. This includes reviewing specialties, medical treatments, elective hospital admissions, rehabilitative services, home care, and out-of-plan referrals. The UMN also assists with complex cases, internal process development, and educates physicians and team members on utilization review issues. Ensuring smooth transitions and patient satisfaction is key to this role.</p><p><br></p><h2>Responsibilities</h2><ul><li>Review prior authorization requests for medical necessity and appropriateness using standardized criteria.</li><li>Coordinate with Medical Directors/Physicians for requests outside of standard criteria.</li><li>Ensure compliance with federal, state, and contractual guidelines.</li><li>Manage caseload by obtaining necessary documentation and addressing discrepancies.</li><li>Serve as a liaison between Medical Directors, physicians, and office staff.</li><li>Perform evaluation and monitoring of resource utilization such as durable medical equipment and hospitalizations.</li><li>Document department work processes and policy guidelines.</li><li>Promote safe and appropriate coordination of care.</li><li>Identify and develop programs, policies, and procedures for continuous quality improvement.</li><li>Maintain confidentiality according to company and department policies.</li><li>Participate in regular departmental training sessions.</li><li>Coordinate enrollee benefits with providers and external organizations.</li><li>Prepare and present reports on department activities.</li></ul><h2>Essential Skills</h2><ul><li>Clinical review</li><li>Utilization review</li><li>Utilization management</li><li>Interqual</li><li>Milliman Commercial Guidelines</li><li>Medicaid</li><li>Medical management</li><li>Medicare</li><li>Managed care</li><li>Patient care</li><li>Medical record management</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Current unrestricted Florida RN or LPN License</li><li>Minimum of two years of utilization review experience</li><li>Minimum of one year of discharge planning experience in an acute care setting</li><li>Four years of related clinical experience in a healthcare field or equivalent education</li><li>Valid Florida Driver’s License</li><li>Knowledge of case management and utilization review concepts</li><li>Familiarity with Florida Medicaid Program and CMS Guidelines</li><li>Proficiency in word processing software, Microsoft Excel, and electronic medical record software</li></ul><h2>Work Environment</h2><p>The role offers a hybrid work schedule post-training, with hours from Monday to Friday, 8am-5pm.</p>

Clinical Review Nurse

<h1 style="font-weight: 700;">Job Title: Clinical Social Worker</h1><br><h2>Job Description</h2><p>We are seeking a compassionate and dedicated Clinical Social Worker to provide direct and indirect services for patients, families, and community members. In this role, you will assist the Behavioral Health Services Coordinator of Social Work in planning and developing programs for specific service populations.</p><br><h2>Responsibilities</h2><ul><li>Provide direct and indirect services to patients, families, and community members.</li><li>Assist in program planning and development for specific service populations.</li><li>Coordinate with families and conduct evaluations.</li><li>Engage in discharge planning and chart reviews.</li><li>Support social service initiatives and behavioral health programs.</li></ul><h2>Essential Skills</h2><ul><li>Master&#39;s Degree in Social Work from an accredited school.</li><li>Certified Clinical Social Worker (CCSW) certification.</li><li>Graduate Social Worker (LGSW) certification.</li><li>CPR - AHA Healthcare Provider certification.</li><li>Proficiency in discharge planning and social work.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Novice knowledge of basic keyboarding and computer functions.</li><li>Minimal knowledge in software, hardware, or information systems.</li><li>Good communication skills and positive customer relations.</li><li>Critical analysis and effective organizational skills.</li><li>Comfortable working independently and ability to effect change.</li><li>CJIS Fingerprint clearance.</li></ul><h2>Work Environment</h2><p>The position will be based on the clinic side, rather than in the hospital. Employees can enjoy paid time off while on contract, as well as paid holidays. The work environment is supportive and offers opportunities for professional growth.</p><br>

Clinical Social Worker

<h1><strong>Job Title: Clinical Systems II Contractor</strong></h1><p><br></p><h2>Job Description</h2><p>We are seeking a talented Clinical Systems II Contractor to join our team. This role involves coordinating and executing system plans, establishing objectives, and leading mid to large projects through implementation phases. The ideal candidate will have strong collaboration skills to work effectively with IT teams, internal and external partners, and external entities.</p><p><br></p><h2>Responsibilities</h2><ul><li>Coordinate the development of systems plans, establish objectives, priorities, time allocations, and deadlines.</li><li>Execute on plans and provide regular status reports to keep management informed of progress and project issues.</li><li>Coordinate and collaborate with IT teams/management along with internal and external operational partners, business and clinical, as well as external entities as necessary to lead mid to large projects through the appropriate phases of implementation.</li><li>Direct staff in providing first-line systems software support, troubleshooting and problem resolution services, liaising with corporate IT and software vendors as appropriate.</li><li>Prepare validation documentation for all major products under the responsibility of the Clinical Systems team, following relevant regulatory guidelines and maintaining close collaboration with corporate IT teams.</li><li>Ensure compliance with processes (SOPs) and subsequent documentation of clinical systems, including support documentation.</li><li>Creation of repositories, development/maintenance processes, guidelines, and standards.</li><li>Validation and maintenance of clinical databases.</li><li>Consult with study managers and data managers during the Clinical Database Start-Up Process on design/specification questions.</li><li>Independently lead and manage the User Acceptance Testing (UAT) process with stakeholders by gathering UAT results, then making any necessary database modifications until all problems are fixed.</li><li>Create standard and ad hoc reports.</li></ul><h2>Essential Skills</h2><ul><li>Clinical Data Management</li><li>Medical Device</li><li>Back End Development</li><li>Database Design</li><li>Clinical IT Systems</li><li>Experience in virtualization and storage systems</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>A minimum of a bachelor’s degree in computer science, technical and/or scientific discipline.</li><li>Industry experience in medical technology or pharma is preferred.</li><li>1+ year of experience in clinical data management, preferably device or pharmaceutical clinical trials.</li><li>Experience with back end development, database design, and programming (e.g. SQL, Python, R, PowerBI).</li><li>Proficient in operating computer systems, with knowledge in CTMS, eTMF, DICOM/image management.</li><li>Experienced in validating, qualifying, and auditing vendors, systems, and software.</li></ul><h2>Work Environment</h2><p>The position operates in a collaborative environment where teamwork with IT teams and external partners is crucial. The role may involve working with various computer systems, including CTMS, eTMF, and DICOM/image management technologies. The work environment encourages adherence to guidelines and standards, fostering a culture of compliance and continuous improvement.</p>

Clinical Systems II

<h1><strong>Job Title: Clinician- Open to Entry Level or Experienced!</strong></h1><p><br></p><h2>Job Description</h2><p>Provide a full continuum of therapeutic and clinical services for children, adolescents, adults, and families in various settings throughout Berkshire County. Services include risk assessment, crisis intervention, in-home therapy, family support, and individual and group psychotherapy.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct risk assessments and provide crisis intervention services.</li><li>Deliver in-home therapy sessions to children, adolescents, and families.</li><li>Provide family support and counseling.</li><li>Conduct individual and group psychotherapy sessions.</li><li>Engage in case management and care management duties.</li></ul><h2>Essential Skills</h2><ul><li>Licensed eligible with a Master&#39;s Degree in Social Work, Counseling Psychology, or a related human-services field.</li><li>Eligibility for licensure in Social Work (LCSW) or Mental Health Counseling (LMHC) for outpatient programs.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in case management, care management, and health care.</li><li>Crisis management skills.</li><li>Open to entry-level candidates.</li></ul><h2>Work Environment</h2><p>Work in an outpatient clinic setting, providing behavioral health and addiction services to children and adults. The work schedule is Monday through Friday, 9am to 5pm. Enjoy the benefits of 7 weeks of paid time off and full benefits.</p>

Clinician

<h1 style="text-align: center;"><strong>Clinician</strong></h1><p><br></p><h2>Job Description</h2><p>Provide a full continuum of therapeutic and clinical services for children, adolescents, adults, and families in a variety of settings throughout Berkshire County. Services include risk assessment, crisis intervention, in-home therapy, family support, and individual and group psychotherapy.</p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct comprehensive risk assessments and crisis interventions.</li><li>Provide in-home therapy and family support services.</li><li>Deliver individual and group psychotherapy sessions.</li><li>Manage case and care management responsibilities.</li><li>Offer outpatient services focused on behavioral health and addiction.</li></ul><h2>Essential Skills</h2><ul><li>Eligibility for licensure in Social Work (LCSW) or Mental Health Counseling (LMHC).</li><li>Master&#39;s Degree in Social Work, Counseling Psychology, or other human-services concentration.</li><li>Proficiency in case management, care management, and healthcare.</li><li>Crisis management experience.</li><li>Open to entry-level candidates.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in outpatient settings is beneficial.</li><li>Strong interpersonal and communication skills.</li></ul><h2>Work Environment</h2><p>Work in an outpatient clinic setting with a focus on children and adults dealing with behavioral health and addiction. The schedule is Monday through Friday, 9am-5pm. Enjoy a supportive work environment offering 7 weeks of PTO and full benefits.</p>

<h1 style="font-weight: 700;">Job Title: Clinician</h1><br><h2>Job Description</h2><p>Provide a full continuum of therapeutic and clinical services for children, adolescents, adults, and families in a variety of settings throughout Berkshire County. Services include risk assessment, crisis intervention, in-home therapy, family support, and individual and group psychotherapy.</p><br><h2>Responsibilities</h2><ul><li>Conduct comprehensive risk assessments and crisis interventions.</li><li>Provide in-home therapy and family support services.</li><li>Deliver individual and group psychotherapy sessions.</li><li>Manage case and care management responsibilities.</li><li>Offer outpatient services focused on behavioral health and addiction.</li></ul><h2>Essential Skills</h2><ul><li>Eligibility for licensure in Social Work (LCSW) or Mental Health Counseling (LMHC).</li><li>Master&#39;s Degree in Social Work, Counseling Psychology, or other human-services concentration.</li><li>Proficiency in case management, care management, and healthcare.</li><li>Crisis management experience.</li><li>Open to entry-level candidates.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in outpatient settings is beneficial.</li><li>Strong interpersonal and communication skills.</li></ul><h2>Work Environment</h2><p>Work in an outpatient clinic setting with a focus on children and adults dealing with behavioral health and addiction. The schedule is Monday through Friday, 9am-5pm. Enjoy a supportive work environment offering 7 weeks of PTO and full benefits.</p><br>

<p style="text-align: center;"><br></p><p style="text-align: center;">&#127775; Now Hiring: Clinician – Make a Difference from Day One! (Entry-Level or Experienced Welcome!) &#127775;</p><p style="text-align: center;"><br></p><p>&#128233;<strong><em>Submit your resume to Nicampana@actalentservices.com!</em></strong></p><p style="text-align: center;"><br></p><p style="text-align: center;"><br></p><p><strong>Location:</strong> Beautiful Berkshire County</p><p><strong>Schedule: </strong>Monday–Friday, 9am–5pm</p><p><strong>Perks:</strong> 7 Weeks Paid Time Off + Full Benefits</p><p>Are you passionate about helping others and ready to launch or elevate your career in mental health? Join a mission-driven team that’s transforming lives across Berkshire County! </p><h3>&#128188; What You’ll Do:</h3><ul><li>Be a frontline hero—conduct risk assessments and provide crisis intervention when it matters most.</li><li>Deliver in-home therapy and support to children, teens, and families.</li><li>Facilitate individual and group therapy sessions that foster healing and growth.</li><li>Offer family counseling and wraparound support services.</li><li>Collaborate on case and care management to ensure holistic, client-centered care.</li></ul><h3>&#129504; What You Bring:</h3><ul><li>A Master’s Degree in Social Work, Counseling Psychology, or a related human services field.</li><li>License-eligible (LCSW or LMHC) or already licensed? Even better!</li><li>Strong communication skills, empathy, and a desire to grow in a supportive environment.</li><li>Experience in crisis management or case management is a plus—but not required.</li></ul><h3>Why You’ll Love It Here:</h3><ul><li>Impact:Every day, your work will directly improve lives.</li><li>Support:Join a collaborative, inclusive team that values your voice.</li><li>Balance:Enjoy a consistent weekday schedule and generous time off.</li><li>Growth:We invest in your development with training, supervision, and advancement opportunities.</li></ul><hr><h1><br></h1>

<p style="text-align: center;">&#127775; Now Hiring: Clinician – Make a Difference from Day One! (Entry-Level or Experienced Welcome!) &#127775;</p><p><strong>Location:</strong> Beautiful Berkshire County</p><p><strong>Schedule: </strong>Monday–Friday, 9am–5pm</p><p><strong>Perks:</strong> 7 Weeks Paid Time Off + Full Benefits</p><p>Are you passionate about helping others and ready to launch or elevate your career in mental health? Join a mission-driven team that’s transforming lives across Berkshire County! </p><h3>&#128188; What You’ll Do:</h3><ul><li>Be a frontline hero—conduct risk assessments and provide crisis intervention when it matters most.</li><li>Deliver in-home therapy and support to children, teens, and families.</li><li>Facilitate individual and group therapy sessions that foster healing and growth.</li><li>Offer family counseling and wraparound support services.</li><li>Collaborate on case and care management to ensure holistic, client-centered care.</li></ul><h3>&#129504; What You Bring:</h3><ul><li>A Master’s Degree in Social Work, Counseling Psychology, or a related human services field.</li><li>License-eligible (LCSW or LMHC) or already licensed? Even better!</li><li>Strong communication skills, empathy, and a desire to grow in a supportive environment.</li><li>Experience in crisis management or case management is a plus—but not required.</li></ul><h3>&#127752; Why You’ll Love It Here:</h3><ul><li>Impact:Every day, your work will directly improve lives.</li><li>Support:Join a collaborative, inclusive team that values your voice.</li><li>Balance:Enjoy a consistent weekday schedule and generous time off.</li><li>Growth:We invest in your development with training, supervision, and advancement opportunities.</li></ul><hr><h1><br></h1>

<h1><strong>Job Description: CMM Operator</strong></h1><p>Looking for someone who can operate CMM Machines and do occasional edits. Zeiss/Calypso software preferred.</p><h2>Responsibilities</h2><ul><li>Operate CMM machines to measure and inspect precision parts and components.</li><li>Interpret engineering drawings, blueprints, and GD&amp;T symbols.</li><li>Create and modify CMM programs using software such as PC-DMIS, Calypso, or MODUS.</li><li>Perform in-process and final inspections to ensure parts meet dimensional tolerances.</li><li>Document inspection results and maintain detailed records of measurements.</li><li>Collaborate with machinists, engineers, and quality personnel to resolve quality issues.</li><li>Perform first article inspections (FAI), PPAPs, and final part verifications.</li><li>Maintain and calibrate inspection equipment to ensure accuracy and compliance.</li><li>Follow company quality procedures, safety policies, and ISO standards.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in CMM software (e.g., PC-DMIS, Calypso, or similar).</li><li>Strong understanding of GD&amp;T and ability to interpret technical drawings.</li><li>Excellent attention to detail and problem-solving skills.</li><li>Familiarity with other inspection tools (e.g., micrometers, calipers, height gauges).</li><li>Ability to work independently and as part of a team.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>High school diploma or equivalent; technical training or associate’s degree preferred.</li><li>2+ years of experience operating and programming CMMs in a manufacturing environment.</li><li>Experience in aerospace, medical device, or automotive industries.</li><li>Knowledge of ISO 9001 and/or AS9100 quality systems.</li></ul>

Cmm Operator Programmer

<h1 style="font-weight: 700;">Job Title: CMM Programmer</h1><br><h2>Job Description</h2><p>We are seeking an experienced CMM Programmer with expertise in using PC-DMIS software. The ideal candidate will have a comprehensive understanding of GD&amp;T, be adept at programming complex parts, and possess machining experience to thrive in a machine shop environment.</p><br><h2>Responsibilities</h2><ul><li>Interpret engineering drawings, specifications, and GD&amp;T requirements to create effective and efficient CMM programs.</li><li>Develop, modify, and optimize CMM programs using PC-DMIS software.</li><li>Design and develop CMM fixturing and tooling to streamline setups.</li><li>Execute CMM programs and analyze results to ensure compliance with quality standards.</li><li>Conduct first-article and in-process inspections.</li><li>Mark parts effectively with machining moves to meet customer specifications.</li><li>Collaborate with engineering and production teams to troubleshoot measurement issues and implement corrective actions.</li><li>Train and mentor staff on CMM programming and measurement techniques as needed.</li><li>Participate in continuous improvement initiatives to enhance measurement processes and efficiency.</li><li>Complete 100% dimensional layouts for PPAP as required.</li><li>Operate multiple CMMs simultaneously to support production checks during the shift.</li><li>Perform routine maintenance and calibration of CMM equipment to ensure accuracy and reliability.</li><li>Stay updated with advances in CMM technologies and measurement techniques.</li></ul><h2>Essential Skills</h2><ul><li>Degree in Manufacturing Engineering, Quality Assurance, or a related field, or equivalent work experience.</li><li>Proven experience as a CMM programmer using PC-DMIS software for complex parts.</li><li>Strong understanding of geometric dimensioning and tolerancing (GD&amp;T) principles.</li><li>Familiarity with CAD software and the ability to read technical drawings.</li><li>Excellent analytical and problem-solving skills.</li><li>Attention to detail and commitment to quality standards.</li><li>Effective communication skills and ability to work collaboratively in a team setting.</li><li>Knowledge of statistical process control (SPC) methodologies.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Certification in metrology or quality control (ASQ, Six Sigma, etc.) is a plus.</li><li>Experience with different types of measuring equipment, such as laser scanners and optical comparators, is desirable.</li><li>Knowledge of casting and machining.</li></ul><h2>Work Environment</h2><p>The work environment includes a quality lab equipped with four CMMs, where 90% of the workday will be spent. The lab is air-conditioned and clean, while the shop floor is a CNC machine shop with multiple buildings. The plant is air-conditioned and well-lit, except for the shipping dock. The position involves working five days a week with flexible hours, including options such as 5am-1:30pm, 6am-2:30pm, or 7am-3:30pm. No overtime is required, and an unpaid lunch break is included. A CMM Operator will assist in this role. The company operates two shifts: 5am-3:30pm and 3:30pm-2am.</p><br>

Cmm Programmer

<h3>Job Summary:</h3><p>We are seeking a motivated and detail-oriented Entry-Level Construction Material Testing Technician to join our team. In this role, you will assist in performing field and laboratory tests on construction materials such as soil, concrete, asphalt, and aggregates to ensure compliance with project specifications and industry standards.</p><hr><h3>Key Responsibilities:</h3><ul><li>Perform field testing of soil, concrete, asphalt, and other construction materials.</li><li>Collect and prepare samples for laboratory testing.</li><li>Conduct on-site inspections and document observations.</li><li>Record and report test results accurately and in a timely manner.</li><li>Maintain testing equipment and ensure calibration standards are met.</li><li>Follow safety protocols and company procedures at all times.</li><li>Communicate effectively with project managers, engineers, and contractors.</li></ul><hr><h3><br></h3>

Cmt Technician

<h1><strong>Job Title: CMT Technician</strong></h1><p><br></p><h2>Job Description</h2><p>Candidates will be responsible for field testing of soils, concrete, and asphalt. LabCAT, American Concrete Institute (ACI) Level I, and WAQTC certifications are desired, though training will be provided for the appropriate candidate. </p><p><br></p><p>This position requires the ability to lift and carry heavy materials. Candidates must have a valid driver&#39;s license with a clean driving record and must pass a <span style="color: rgb(8, 7, 7); background-color: none;">background</span> check. </p><p><br></p><h2>Responsibilities</h2><ul><li>Conduct field testing of soils, concrete, and asphalt.</li><li>Handle and transport testing materials safely.</li><li>Work with scheduling and oversight of the CMT team.</li><li>Engage in all client interactions professionally.</li><li>Work on a variety of projects, primarily vertical construction but also including renewables and transportation.</li></ul><h2>Essential Skills</h2><ul><li>0 to 1 year experience as a CMT technician</li><li>ACI is a plus</li><li>Experience in soil and concrete testing.</li><li>Ability to pass a drug and <span style="color: rgb(8, 7, 7); background-color: none;">background</span> check.</li><li>Clean Motor Vehicle Record (MVR).</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>LabCAT, ACI Level I, and WAQTC certifications a plus</li><li>Strong interpersonal skills to work with multiple personalities.</li><li>Self-starter with a proactive attitude.</li></ul><h2>Work Environment</h2><p>The company operates in Colorado with offices in South Denver, Parker, Colorado Springs. Employees work on a variety of projects, mainly vertical construction but also renewables and transportation. The role typically does not require weekend work. Employees have the opportunity to earn 5+ hours of overtime regularly. </p>

<h1><strong>Actalent is looking for a CNC Programmer II to join our Medical Device Client!</strong></h1><p><br></p><h2>Job Description</h2><p>The CNC Programmer II will be responsible for creating and revising CNC programs, designing and validating multi-step machining operations, and designing and sourcing custom fixturing. The role also involves supporting current production and prototype projects while maintaining quality and safety standards, and creating and managing engineering documents including drawings, inspection documents, tool layouts, offset sheets, operator and setup instructions.</p><p><br></p><h2>Responsibilities</h2><ul><li>Create and revise CNC programs for multi-step machining operations.</li><li>Design and source custom fixturing for manufacturing processes.</li><li>Support production and prototype projects while adhering to quality and safety standards.</li><li>Manage engineering documents such as drawings, inspection documents, tool layouts, offset sheets, operator and setup instructions.</li></ul><h2>Essential Skills</h2><ul><li>Proficiency in CNC programming, particularly with Multi Axis Swiss Lathe.</li><li>Experience in programming using Esprit software.</li><li>Understanding of Geometric Dimensioning and Tolerancing (GD&amp;T).</li><li>3-5 years of experience in programming Multi Axis Swiss machines.</li><li>5 Axis experience is required.</li><li>Knowledge of part manufacturing, machine setup, and part programming in manufacturing process development.</li><li>Proficient with computer software including SolidWorks, Microsoft Excel, AutoCAD, and/or PartMaker.</li><li>Knowledge of fixture design and manufacturing.</li><li>Proficient in G code programming and using CAM software.</li><li>Full understanding of tooling applications including speed and feeds.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience in the aerospace industry is beneficial.</li></ul><h2>Work Environment</h2><p>Enjoy a four-day work week from Monday through Thursday on the first shift. Work with advanced equipment such as Multi Axis Swiss Lathes and 3, 4, and 5 Axis Mills.</p>

Cnc Programmer

<h1><strong>Job Title: CNC Programmer</strong></h1><h2>Job Description</h2><p>We are seeking an experienced CNC Programmer to write machining programs using Esprit and/or Mastercam CAM software. The role involves providing technical expertise and support to the production floor, as well as process documentation to the planning department, including set-up sheets, perishable tooling, and in-process inspection requirements. The ideal candidate will investigate process problems affecting manufacturing and quality assurance and recommend improvements to enhance performance, increase reliability, and decrease costs.</p><p><br></p><h2>Responsibilities</h2><ul><li>Write machining programs using Esprit and/or Mastercam CAM software.</li><li>Provide technical expertise and support to the production floor.</li><li>Supply process documentation, including set-up sheets, perishable tooling, and in-process inspection requirements to the planning department.</li><li>Investigate and resolve process problems affecting manufacturing and quality assurance.</li><li>Recommend improvements to manufacturing processes for better performance, reliability, and cost-efficiency.</li></ul><h2>Essential Skills</h2><ul><li>10+ years of experience in programming multi-axis CNC lathes in a manufacturing environment.</li><li>5+ years of experience in Aerospace.</li><li>Proficiency in machining materials from aluminum, stainless steel, titanium, and alloy steels.</li><li>Familiarity with ISO 9001 and/or AS9100 quality systems and documentation.</li></ul><h2>Additional Skills &amp; Qualifications</h2><ul><li>Experience with CNC lathe and/or mill operations.</li><li>Proficiency in using Mastercam and/or Esprit software.</li></ul><h2>Work Environment</h2><p>The work environment is dynamic and fast-paced, with new projects frequently coming in, ensuring a constant flow of work. The company supports high performance engine components for various industries, including motorsports, aerospace, defense, space, and medical sectors. Programmers have their own dedicated space and work closely with quality and process engineers, developing fixtures and collaborating with the setup team. </p>

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