<h1>Job Title: Clinical Data Coordinator</h1> Job DescriptionWe are seeking a dedicated Clinical Data Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves coordinating the preparation of study tools, collaborating with research nurses and physicians, and ensuring compliance with protocols. Responsibilities<ul><li>Coordinate the initiation and activation of all new clinical trial protocols.</li><li>Prepare study tools including study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word.</li><li>Review patients&#39; charts and medical history to confirm protocol eligibility and obtain necessary source documents.</li><li>Ensure that IRB approved informed consent forms are obtained, signed, and properly filed.</li><li>Maintain research records for all patients enrolled in studies, including patient consent, eligibility, CRFs, and source documents.</li><li>Assist with grading adverse events using NCI common toxicity criteria and complete SAE forms as required.</li><li>Provide regular reports to tumor study group members and Principal Investigators using Oncore®.</li><li>Serve as a liaison with study sponsors, schedule monitoring visits, and respond to sponsors&#39; queries.</li></ul>Essential Skills<ul><li>Coordinator experience in oncology.</li><li>Clinical research experience with 1-2 years primarily focused on data entry and query resolution for oncology trials.</li></ul>Additional Skills &amp; Qualifications<ul><li>IATA certification.</li><li>Experience in screening, enrolling, and consenting patients into research studies based on study protocols.</li><li>Experience in medication administration and adverse event reporting.</li><li>Requiring 1-2 years of CRC or data coordinating experience</li></ul> Work Environment<ul><li>The position is based in an NCI Designated Cancer Center, requiring 1-2 years of CRC experience in oncology.</li><li>The role involves regular interactions with study sponsors and requires a professional dress code.</li></ul>

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Clinical Data Coordinator

<h1 style="font-size: 2em; font-weight: normal;">Microbiologist</h1> Job DescriptionWe are seeking a dedicated and skilled Microbiologist to lead experimental execution and research projects. You will design and execute experiments independently or collaboratively, adhering to scientific protocols and methodologies. Your expertise will ensure the accuracy and reliability of experimental results, while you provide guidance and direction to project teams in a collaborative research environment. Responsibilities<ul><li>Design and execute experiments, ensuring adherence to scientific protocols and methodologies.</li><li>Perform laboratory techniques and procedures accurately, including sample preparation and data analysis.</li><li>Oversee small projects or programs, directing assignments of other staff members.</li><li>Serve as the responsible person for operation, maintenance, and troubleshooting of complex equipment.</li><li>Lead and manage scientific research projects, ensuring alignment with organizational goals.</li><li>Analyze experimental data using statistical software, interpreting results, and drawing conclusions.</li><li>Prepare technical reports, presentations, and scientific publications for internal and external audiences.</li><li>Develop and improve methods, test plans, and experimental designs.</li><li>Coordinate cross-functional project teams to achieve project objectives.</li><li>Maintain accurate records of experimental procedures, observations, and results.</li><li>Collaborate with multidisciplinary teams to drive scientific innovation.</li><li>Communicate research findings and project status effectively to senior scientists and project leaders.</li><li>Adhere to quality control measures and standard operating procedures.</li><li>Identify opportunities for process improvement and innovation in research methodologies.</li></ul> Essential Skills<ul><li>Degree in Microbiology with at least 3 years of experience as a Microbiologist in a hospital setting.</li><li>Proficiency in microbiology, laboratory techniques, and mass spectrometry.</li><li>Experience with MALDI and MALDI-TOF.</li><li>Strong technical leadership and mastery in protocol troubleshooting and optimization.</li><li>Evidence of potential for original or collaborative research leading to publication.</li></ul> Additional Skills &amp; Qualifications<ul><li>Master&#39;s Degree with clinical microbiology experience, or Bachelor&#39;s Degree with at least 4 years of experience.</li><li>American Society for Clinical Pathology (ASCP) Certified Medical Laboratory Scientist (MLS).</li><li>Proven track record of contributing to scientific research through peer-reviewed publications and patented work.</li></ul> Work EnvironmentThis role offers the opportunity to make a significant impact as the solo microbiologist on the team. You will be the key person for all microbiology-related matters, working in a collaborative environment to advance scientific research and innovation.

Clinical Lab - Microbiologist

<h1 style="font-size: 2em; font-weight: normal;">Clinical Lab Analyst</h1> Job DescriptionAs a Clinical Lab Analyst, you will perform newborn screening testing on blood spot specimens to help identify infants at risk for inherited conditions. Your role involves using various methods such as immunoassay, enzyme assay, electrophoresis, HPLC, tandem mass spectrometry, and molecular methods to ensure accurate screening results. Responsibilities<ul><li>Perform daily operation and routine maintenance, calibration, and assist in troubleshooting of laboratory instruments and equipment.</li><li>Document and review newborn screening test data, procedures, and results.</li><li>Release data and reports for use by physicians, health care professionals, and newborn screening medical follow-up personnel.</li><li>Develop and maintain standard operating procedures and prepare documentation for test verification or validation studies.</li><li>Perform quality control and quality assurance procedures in accordance with established standard operating procedures and policies.</li><li>Recognize basic problems and assist troubleshooting of laboratory method and performance issues.</li><li>Assemble quality control data for further analysis; recognize problems; document issues; perform root cause analysis; and initiate corrective actions.</li></ul>Essential Skills<ul><li>Proficiency in chemistry, biology, genetics, HPLC, mass spectrometry, and biochemistry.</li><li>Bachelor’s degree in Chemistry, Biochemistry, Biology, Genetics, or related field, or equivalent combination of education and experience.</li><li>Meet Clinical Laboratory Improvement Amendments (CLIA) qualifications for high complexity testing (6 semesters of Biology and 6 semesters of Chemistry).</li><li>At least 3 months of hands-on laboratory experience.</li><li>Consideration given to certified Medical Lab Technologist or MLT.</li></ul>Additional Skills &amp; Qualifications<ul><li>Six months to one year of newborn screening laboratory experience.</li><li>Basic experience with immunoassay, mass spectrometry, and molecular biology techniques.</li><li>Completion of human genetics college coursework.</li><li>Quality Assurance and Quality Control (QA/QC) experience.</li></ul>Work EnvironmentWork in a lab where newborn blood samples are tested for potential inherited disorders. This department operates 24/7 to ensure timely testing. The lab, located in Ankeny, tests samples from Iowa, North Dakota, South Dakota, and Alaska. The job involves working the 1st shift from 8 AM to 4:30 PM with rotating weekends and holidays, where weekend shifts are 7 AM to 3:30 PM. The position is a 4-month contract during a leave of absence. Dress code includes long pants and closed-toed shoes.

Clinical Lab Analyst

<h1 style="font-size: 2em; font-weight: normal;">**Clinical Research Assistant / Study Coordinator**</h1>Job DescriptionWe are seeking a dedicated Study Coordinator to conduct human subject research, focusing on wearable devices in an exercise setting. The role involves monitoring participants, collecting data, and ensuring the smooth operation of technology products throughout the study. Responsibilities<ul><li>Conduct research with human participants using wearable devices in an exercise setting.</li><li>Monitor and collect data throughout the study sessions, each lasting up to 2.5 hours.</li><li>Consent participants and take necessary vitals and measurements, such as height, weight, and EKG.</li><li>Ensure proper setup of devices and monitoring equipment for participants.</li><li>Observe participants using devices according to protocol and ensure data monitoring functions properly.</li><li>Collect data through equipment and manually, ensuring accuracy and completeness.</li><li>Guide participants throughout the study and provide necessary support.</li></ul>Essential Skills<ul><li>Bachelor&#39;s degree in Science, Exercise Science, Kinesiology, or Biology.</li><li>Technical proficiency with test devices and data entry.</li><li>Ability to stand for an entire shift and familiarity with gym equipment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in human subject research and data analysis.</li><li>Experience as a personal trainer.</li></ul>Work EnvironmentThe position offers flexible shifts, with options for AM (7:30 AM to 3:00 PM) or PM (2:00 PM to 9:00 PM) shifts, and the possibility of double shifts. Dress code is casual but presentable. The study may include outdoor activities, and training is typically conducted during the day but can be accommodated for evening shifts if needed. The study will run through the end of the year, with potential continuation into early next year. Job Type &amp; LocationThis is a Contract position based out of Natick, Massachusetts.

Clinical Research Assistant

<h1>**Clinical Research Assistant / Study Coordinator**</h1>Job DescriptionWe are seeking a dedicated Study Coordinator to conduct human subject research, focusing on wearable devices in an exercise setting. The role involves monitoring participants, collecting data, and ensuring the smooth operation of technology products throughout the study. Responsibilities<ul><li>Conduct research with human participants using wearable devices in an exercise setting.</li><li>Monitor and collect data throughout the study sessions, each lasting up to 2.5 hours.</li><li>Consent participants and take necessary vitals and measurements, such as height, weight, and EKG.</li><li>Ensure proper setup of devices and monitoring equipment for participants.</li><li>Observe participants using devices according to protocol and ensure data monitoring functions properly.</li><li>Collect data through equipment and manually, ensuring accuracy and completeness.</li><li>Guide participants throughout the study and provide necessary support.</li></ul>Essential Skills<ul><li>Bachelor&#39;s degree in Science, Exercise Science, Kinesiology, or Biology.</li><li>Technical proficiency with test devices and data entry.</li><li>Ability to stand for an entire shift and familiarity with gym equipment.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience in human subject research and data analysis.</li><li>Experience as a personal trainer.</li></ul>Work EnvironmentThe position offers flexible shifts, with options for AM (7:30 AM to 3:00 PM) or PM (2:00 PM to 9:00 PM) shifts, and the possibility of double shifts. Dress code is casual but presentable. The study may include outdoor activities, and training is typically conducted during the day but can be accommodated for evening shifts if needed. The study will run through the end of the year, with potential continuation into early next year. Job Type &amp; LocationThis is a Contract position based out of Natick, Massachusetts. Please send your resume and 2 professional references to hjaquez @actalentservices.com for next steps.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator </h1> Job DescriptionThe Research Coordinator will play a vital role in assisting an Investigator, Research Associate, or Project Manager with the operational tasks necessary for implementing a research study. This position involves various responsibilities related to participant recruitment, data collection, data management, and reporting of study results. Responsibilities<ul><li>Recruit and obtain consent from research participants.</li><li>Conduct telephone or in-person interviews, including eligibility screening.</li><li>Perform follow-up with study participants via telephone, e-mail, 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><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul>Required Skills &amp; Qualifications<ul><li>High school diploma or General Education Development (GED)</li><li>6+ months of clinical research experience</li><li>Backgroundin the medical field, including phlebotomy and vaccines</li><li>Tech-savvy</li><li>Interest in growing in clinical research</li><li>Data entry skills</li></ul>

Clinical Research Coordinator

SR CLINICAL RESEARCH COORDINATOR Job DescriptionWe 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. As a subject/patient-facing position, strong communication skills are essential for collecting detailed clinical information and sharing it with the study team. The coordinator will be responsible for all aspects of trial conduct, including IRB submission, regulatory documentation, staff training, and overseeing subject enrollment. Responsibilities<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><li>Oversee the ordering, receipt, and maintenance of study supplies.</li><li>Communicate regular study updates with administration.</li><li>Oversee clinic activities as assigned.</li><li>Perform clinical activities as experience and delegation allow.</li><li>Perform on-call duties during evenings and weekends as assigned.</li></ul>Essential Skills<ul><li>Clinical research coordination, screening, enrolling, and regulatory knowledge.</li><li>Proficiency in Microsoft Office products, including Excel.</li><li>Experience with clinical documentation and HIPAA guidelines.</li><li>RedCap and various clinical databases proficiency.</li><li>3+ years of clinical research experience</li></ul>Additional Skills &amp; Qualifications<ul><li>Associates or Bachelor’s degree in a clinical or scientific field, or clinical certificate/license</li><li>Cardiology experience preferred</li><li>Clinical skills, including phlebotomy, ability to take and record accurate vital signs, obtain EKG tracings, and familiarity with medical terminology preferred.</li><li>Clinical Research certification by SoCRA or ACRP.</li></ul>

<h1>Job Title: Clinical Research Coordinator</h1> Job DescriptionJoin our dynamic team as a Clinical Research Coordinator!$25-27/hr Training will be provided on the first shift for 4-6 weeks to ensure you are well-prepared for the role. You will work with a schedule set 2-3 weeks in advance, ensuring flexibility and planning. Your primary role will be collaborating with Clinical Research Nurses to manage Phase I Clinical Trials. Responsibilities<ul><li>Create e-source documents, labels, and study-specific instructions.</li><li>Host clinical planning meetings for each stage in study start-up.</li><li>Develop study schedules.</li><li>Order supplies, equipment, and dietary needs for studies.</li><li>Liaise with CRU contracted services (e.g., clinical labs, ECG services).</li><li>Train staff on study-specific procedures.</li><li>Coordinate participant check-in, discharge, and issue resolution.</li><li>Complete sample shipment documentation.</li><li>Compile data tables and summaries.</li><li>Ensure timely CRF completion and manage queries.</li><li>Compile protocol and SOP deviations.</li><li>Provide logistical feasibility for protocol development.</li><li>Maintain accurate work records.</li><li>Stay updated on FDA, GCP, and ICH requirements.</li><li>Ensure client and participant confidentiality is maintained.</li><li>Evaluate and revise SOPs.</li><li>Assist with form reviews and activity plans on bedside date capture.</li><li>All other duties as needed or assigned.</li></ul>Additional Skills &amp; Qualifications<ul><li>University/college degree (life science, pharmacy or related subject preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology). (May consider relevant and equivalent experience in lieu of educational requirements.)</li><li>1-2 years of professional work experience with at least 1 year experience in clinical research.</li><li>Basic Life Support Skills (BLS) or CPR/AED Certified.</li></ul>

<h1 style="text-align: center;">Clinical Research Coordinator</h1>Job DescriptionJoin our dynamic research team to assist with study coordination and recruitment for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. You will work closely with study physicians, research coordinators, project managers, and other research staff to advance our research mission within a vibrant Division. Responsibilities<ul><li>Assist with study coordination and recruitment for various research projects.</li><li>Work directly with study physicians, research coordinators, project managers, and other research staff.</li><li>Perform screening visits and consent participants for studies.</li><li>Process and ship laboratory samples.</li><li>Enter data into databases accurately and efficiently.</li><li>Escort participants to other testing and procedure areas.</li></ul>Essential Skills<ul><li>Experience in clinical research, patient enrollment, and recruitment.</li><li>Proficiency in chart review and data entry.</li><li>Ability to pre-screen patients effectively.</li><li>Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB), and Electronic Data Capture (EDC) systems.</li></ul>Additional Skills &amp; Qualifications<ul><li>1-2 years of related experience or an equivalent combination of education and experience.</li></ul>Work EnvironmentThis role offers flexibility with work-from-home options: the first week is on-site, with one day of remote work available during the first four months. After establishing your role, two days of remote work are possible, as long as it does not interfere with departmental operations. The work location is conveniently situated near public transportation options, including PATCO and SEPTA, with parking available. The team is diverse and well-supported, fostering a collaborative and fulfilling work environment. You will work on high-profile studies, including drug trials for movement disorders such as Parkinson&#39;s disease, within a recognized Center of Excellence. The opportunity is both challenging and rewarding, with the chance to contribute significantly to research that impacts lives. Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for more information.

Clinical Research Coordinator (Contract Position) Duration: Scoped through December 2026Job Type: 40 hours per week (Monday-Friday) - during normal business hoursStart Date: ASAP Job Description:We are seeking a full-time, onsite Clinical Research Coordinator (CRC) with experience in clinical research to support an ongoing Oncology clinical trial. Key Responsibilities:<ul><li>Patient Recruitment</li><li>Medical Record Review</li><li>Participant Screening</li><li>Informed Consent</li><li>Data Management &amp; query resolution</li><li>Medical Record Retrieval</li><li>Regulatory Support: Assist with Institutional Review Board (IRB) approvals and provide regulatory support.</li><li>Adverse Event Reporting: Assist with timely reporting of adverse events (AEs) and serious adverse events (SAEs).</li><li>Study Binder Maintenance: Keep study binders organized and up-to-date.</li><li>Participant Follow-Up: Conduct follow-up with study subjects to ensure retention.</li><li>Scheduling: Arrange in-patient visits and follow-up appointments, and send reminders.</li><li>Administrative Tasks: Perform various administrative duties as required.</li><li>Community Outreach: Networking with referral physicians, visiting clinics and hospitals to educate medical professionals and patients about the clinical trial, distributing study materials, posting recruitment materials, and maintaining online portals to track metrics.</li><li>General Support: Assist with any other study-related efforts as deemed necessary by the site.</li></ul> Qualifications:<ul><li>Minimum of two years of experience as a Clinical Research Coordinator</li><li>Oncology experience preferred</li><li>Proficiency with electronic medical records (EMR) and electronic data capture (EDC) system</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator</h1> Job DescriptionWe are seeking a Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves verifying approvals from various committees, preparing study tools, and ensuring compliance with study protocols. Responsibilities<ul><li>Coordinate the initiation and activation of all new clinical trial protocols, ensuring necessary approvals and documentation are in place.</li><li>Prepare study tools such as binders, medication diaries, eligibility checklists, and flow sheets.</li><li>Collaborate with Research Nurse Clinicians and physicians to review patient charts and confirm protocol eligibility.</li><li>Ensure informed consent forms are obtained and documented properly.</li><li>Register consented research patients with study sponsors and input data into the clinical trials database.</li><li>Maintain comprehensive research records for all patients enrolled in clinical trials.</li><li>Assist in grading adverse events and complete necessary forms for serious or unexpected adverse events.</li><li>Provide regular reports to study group members and Principal Investigators.</li><li>Serve as a liaison with study sponsors, schedule monitoring visits, and respond to queries.</li><li>Ensure studies are conducted according to treatment plans and Good Clinical Practice (GCP) guidelines.</li></ul>Essential Skills<ul><li>1-3 years of experience as a Clinical Research Coordinator.</li><li>Proficiency in clinical research, oncology, and informed consent processes.</li><li>Ability to recruit, enroll, and manage source documents for patients.</li><li>Experience with software programs such as Excel®, Word®, and Access®.</li><li>Strong organizational, communication, and interpersonal skills.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor&#39;s Degree required.</li><li>Detail-oriented with the ability to maximize resources and be resourceful.</li><li>Commitment to high standards of professional excellence and accountability.</li></ul>Work EnvironmentThis position is part of a Clinical Operations team comprising 40 FTEs across various disease-specific groups, including breast, lung, phase 1, and GI. The team operates in multiple sites, including Newark, with a goal to enroll 5,000 subjects per year across 300 active trials. The work environment includes collaboration with RA, QA, Informatics, Education, and Finance departments, aiming for a long-term goal of 2,500 active subjects across all phases of adult and pediatric trials. Job Type &amp; LocationThis is a Contract to Hire position based out of New Brunswick, New Jersey.

Description
					Research Data Coordinator part of the data core team. Supporting with data entry for oncology trials. 
Cancer center is transitioning to electronic system; there is a bit of scanning paper documents and using them on source documents
					Skills
					clinical research, electronic medical record, oncology
					Top Skills Details
					clinical research,electronic medical record
					Additional Skills &amp; Qualifications
					understands medical terminology and extract data from a database like Epic and extract the data
experience: if they have spent 1-1.5year in medicine, anything related to cancer (should know where to get information) 
source document verification 
having good quality source docs
Epic – know it, know where to find stuff

SOFT SKILLS:
Friendly, gets along with others
Understands the transition from paper to electronic and help people get there 
Communication between clinical care people and research 
Positive and good transition 
(great for people that have already been electronic)
					Experience Level
					Intermediate Level

<h1>Job Title: Clinical Research Coordinator - Rocky Mount, NC</h1>Job DescriptionThe Research Coordinator will assist an Investigator, Research Associate, or Project Manager in executing tasks essential for conducting a research study. This involves various responsibilities related to recruitment, data collection, data management, and the reporting of results. Responsibilities<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 via 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><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Manage bookkeeping related to study budgets, such as ordering supplies and requesting checks for payment and participant incentives.</li><li>Handle miscellaneous administrative tasks, including typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul> Essential Skills<ul><li>High school diploma or General Education Development (GED).</li><li>At least 6 months of clinical research experience.</li><li>Experience in the medical field, including phlebotomy and vaccine knowledge.</li></ul> Additional Skills &amp; Qualifications<ul><li>Tech-savvy with an interest in growing in Clinical Research.</li><li>Proficiency in data entry.</li></ul> Work EnvironmentThe position is based on-site for 5 days a week. You will have the opportunity to support one of the leading healthcare providers in the US and work in clinical research trials. Job Type &amp; LocationThis is a Contract position based out of Rocky Mount, North Carolina.

<h1>Job Title: Research Coordinator</h1>Job DescriptionThe Research Coordinator will support the implementation of research studies by assisting an Investigator, Research Associate, or Project Manager. This role involves recruitment, data collection, data management, and results reporting, contributing significantly to the success of clinical research trials. Responsibilities<ul><li>Recruit and consent research participants.</li><li>Conduct telephone or in-person interviews with participants, including eligibility screening.</li><li>Perform follow-up via telephone, email, and mail with study participants.</li><li>Prepare, mail, and process questionnaires and other study correspondence.</li><li>Assist in tracking study participants using MS Excel.</li><li>Maintain accurate and detailed records and files of work.</li><li>Review, edit, clean, and enter participant data into a database.</li><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Manage bookkeeping related to study budgets, including ordering supplies and requesting checks for payments and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul>Essential Skills<ul><li>High school diploma or General Education Development (GED).</li><li>6+ months of clinical research experience.</li><li>Experience in the medical field, including phlebotomy and vaccine knowledge.</li></ul> Additional Skills &amp; Qualifications<ul><li>Tech-savvy with a strong interest in growing in clinical research.</li><li>Proficiency in data entry.</li><li>Experience with chart review, patient recruitment, EDC, EMR, and GCP.</li></ul> Work EnvironmentThis position requires working 5 days on-site in Bristol, Tennessee. The role offers an opportunity to support one of the leading healthcare providers in the US and engage in clinical research trials. Job Type &amp; LocationThis is a Contract position based out of Bristol, Tennessee.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator</h1>Job DescriptionJoin our team as a Clinical Research Coordinator, where you will play a pivotal role in performing ultrasound imaging for research participants during scheduled onsite visits. Collaborate closely with clinical and research teams to gather, document, and manage imaging and clinical data, ensuring the accurate and timely entry of results into study databases. Support patient recruitment efforts, including outreach, screening, and scheduling, while maintaining compliance with study protocols and regulatory requirements.Responsibilities<ul><li>Perform ultrasound imaging for research participants during scheduled onsite visits.</li><li>Collaborate with clinical and research teams to gather, document, and manage imaging and clinical data.</li><li>Ensure accurate and timely entry of results into study databases.</li><li>Support patient recruitment efforts, including outreach, screening, and scheduling.</li><li>Maintain compliance with study protocols and regulatory requirements.</li></ul>Essential Skills<ul><li>2-3 years of experience in a related field.</li><li>Current GCP and IATA certifications.</li><li>Proficiency in phlebotomy.</li><li>Strong data management skills.</li><li>Excellent people skills and highly organized.</li><li>Good with paperwork and data entry.</li></ul>Additional Skills &amp; Qualifications<ul><li>Oncology background preferred, not required.</li><li>Bachelor&#39;s degree preferred, not required (years of experience can compensate).</li></ul>Work EnvironmentThis is a fully onsite opportunity based in Haverford, PA, where you will support a women&#39;s health clinic focused on a breast cancer device trial. Work onsite 5 days per week, ensuring high enrollment in trials. Enjoy 1 week of PTO and 6 holidays as part of our supportive team environment. Job Type &amp; LocationThis is a 12-month contract position based out of Haverford, Pennsylvania.

The Clinical Data Coordinator will coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects. Create informational and recruitment materials and act as a liaison for the purpose of implementation of studies. The CDC will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and coordinate operational efforts. Assure compliance with state and federal regulatory guidelines. Oversee the quality of the medical and clinical research data. Provide direction and guidance to investigators. Assist PIs with proposals, progress reports and manuscripts. Independently create original documents and policies for assigned disease teams. Work closely with federal and state regulatory officials.<h1>MINIMUM QUALIFICATIONS</h1><ul><li>1-2 years of related experience and a Bachelor’s degree in related area </li><li>Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.</li><li>Experience with EMR and EDC systems</li><li>Oncology experience is preferred</li><li>Understanding of medical terminology</li></ul>WORK ENVIRONMENT<ul><li>This is an on-site position in San Diego (5 days per week). The schedule will be Monday-Friday 8am-5pm. </li></ul>

Job Title: Clinical Research Coordinator – Oncology Trials Data CoordinationDescription: Join a dynamic data core team supporting oncology clinical trials. This role focuses on data entry and source document verification, contributing to the transition from paper-based records to an electronic system. Responsibilities include scanning paper documents, integrating them into electronic source documents, and ensuring high-quality data management.Key Responsibilities:<ul><li>Perform data entry and source document verification for oncology trials</li><li>Extract and validate data from electronic medical records (e.g., Epic)</li><li>Support the transition from paper to electronic documentation</li><li>Collaborate with clinical and research teams to ensure data accuracy and completeness</li></ul>Required Skills:<ul><li>Clinical research experience</li><li>Familiarity with electronic medical records (Epic preferred)</li><li>Understanding of medical terminology</li><li>Ability to locate and extract relevant data from EMRs</li><li>Experience with oncology or cancer-related research is highly desirable</li></ul>Soft Skills:<ul><li>Friendly and collaborative team player</li><li>Strong communication skills across clinical and research teams</li><li>Positive attitude toward change and technology adoption</li><li>Adaptable and supportive during system transitions</li></ul>Experience Level: Intermediate – Ideal candidates will have 1 to 1.5 years of experience in a medical or clinical research setting, particularly in oncology.

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator</h1> Job DescriptionThe Clinical Research Coordinator will play a pivotal role in patient-facing activities, including screening, recruitment, and managing source documentation. The role requires documenting in Electronic Medical Records (EMR) and ordering labs. You will work in collaboration with a team responsible for specimen collection and processing, allowing you to focus on managing patient interactions without data entry responsibilities. Your main responsibilities will involve screening, consenting, and enrolling patients in oncology trials, and following them through their therapy course. Responsibilities<ul><li>Screen, consent, and enroll patients in oncology trials.</li><li>Follow patients through their therapy course and ensure protocol compliance.</li><li>Spend most of the time in the clinic, seeing patients with doctors and attending patient visits.</li><li>Ensure questionnaires are completed and research procedures outside the clinical norms are done.</li><li>Work with clinic staff to schedule appointments such as EKGs or vitals.</li><li>Interact with nursing staff and medical assistants.</li><li>Collaborate with clinical staff to obtain insurance authorizations.</li><li>Work with infusion nurses to schedule appointments.</li><li>Maintain an enthusiastic attitude.</li></ul>Essential Skills<ul><li>Clinical research experience.</li><li>Pre-screening patients.</li><li>Oncology knowledge.</li><li>Chart review skills.</li><li>Patient recruitment experience.</li><li>Minimum 2 years of Clinical Research Coordinator experience with acute Therapeutic Area experience.</li><li>CRC: 4+ years of oncology CRC experience.</li><li>Bachelor&#39;s degree.</li></ul>Additional Skills &amp; Qualifications<ul><li>Patient study enrollment experience.</li><li>Ability to read protocols and identify side effects.</li><li>Exceptional organizational skills.</li><li>Experience in managing oncology patients.</li><li>Ability to assist patients with various aspects of study participation.</li></ul>Work EnvironmentThe work environment involves participating in pharmaceutical-sponsored trials, acting as one of the sites for Phase I, Phase II, and occasionally Phase III trials. You will collaborate with the Investigator Davis Oncology department, managing INDs and progress reports to the FDA. The clinical group is divided into disease teams, with clinical staff working in the cancer center and data management staff working in a different center. The position requires working Monday to Friday from 8 AM to 5 PM with some flexibility based on the clinic schedule. Office visits are required daily, and the position is on-site. Job Type &amp; LocationThis is a Contract to Hire position based out of Sacramento, California.

<h1>Job Title: Clinical Research Coordinator</h1>Job DescriptionWe are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This role involves assisting in the development and implementation of clinical study protocols, coordinating participant recruitment, and managing daily operations of clinical trials. The ideal candidate will have strong experience in clinical research or healthcare, with a preference for those with phlebotomy experience. Responsibilities<ul><li>Assist in the development and implementation of clinical study protocols.</li><li>Coordinate participant recruitment, screening, and enrollment.</li><li>Manage daily operations of clinical trials, including scheduling and conducting participant visits.</li><li>Serve as a liaison between study participants, investigators, and other healthcare professionals.</li><li>Monitor study progress and report any issues or adverse events to the Principal Investigator and relevant authorities.</li></ul>Essential Skills<ul><li>Phlebotomy experience is highly preferred.</li><li>Previous experience in clinical research or healthcare.</li><li>Strong organizational and communication skills.</li><li>Ability to work independently and as part of a team.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor&#39;s degree in a related field preferred (e.g., life sciences, nursing, public health), but a minimum of a high school diploma is required.</li><li>Experience in patient recruitment, pre-screening, and clinical research, especially in dermatology.</li></ul>Work EnvironmentThis is a fully onsite position, operating Monday through Friday from 8 am to 5 pm EST. Job Type &amp; LocationThis is a Contract to Hire position based out of West Lafayette, Indiana.

<h2>Research Data Coordinator</h2><h3>Overview:</h3>We are seeking a detail-oriented and collaborative Research Data Coordinator to join our Data Core Team supporting oncology clinical trials. This role is pivotal in ensuring accurate and timely data entry, verification, and management as our cancer center transitions from paper-based systems to a fully electronic data environment.<h3>Key Responsibilities:</h3><ul><li>Perform data entry and source document verification for oncology trials.</li><li>Support the transition from paper to electronic systems, including scanning and digitizing paper documents.</li><li>Extract and validate clinical data from electronic health records (EHR) systems such as Epic.</li><li>Ensure high-quality source documentation and maintain data integrity across platforms.</li><li>Collaborate with clinical care teams and research staff to facilitate smooth data workflows.</li><li>Assist in identifying and resolving data discrepancies and support audit readiness.</li></ul><h3>Required Skills &amp; Qualifications:</h3><ul><li>Familiarity with medical terminology, especially in oncology.</li><li>Experience with Epic or similar EHR systems; ability to locate and extract relevant clinical data.</li><li>1–1.5 years of experience in a research or cancer-related setting.</li><li>Strong understanding of source document verification and quality standards.</li><li>Ability to work with both paper and electronic documentation systems.</li></ul>

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator</h1>Job DescriptionJoin our team as a Clinical Research Coordinator, where you will play a pivotal role in performing ultrasound imaging for research participants during scheduled onsite visits. Collaborate closely with clinical and research teams to gather, document, and manage imaging and clinical data, ensuring the accurate and timely entry of results into study databases. Support patient recruitment efforts, including outreach, screening, and scheduling, while maintaining compliance with study protocols and regulatory requirements. Responsibilities<ul><li>Perform ultrasound imaging for research participants during scheduled onsite visits.</li><li>Collaborate with clinical and research teams to gather, document, and manage imaging and clinical data.</li><li>Ensure accurate and timely entry of results into study databases.</li><li>Support patient recruitment efforts, including outreach, screening, and scheduling.</li><li>Maintain compliance with study protocols and regulatory requirements.</li></ul> Essential Skills<ul><li>2-3 years of experience in a related field.</li><li>Current GCP and IATA certifications.</li><li>Proficiency in phlebotomy.</li><li>Strong data management skills.</li><li>Excellent people skills and highly organized.</li><li>Good with paperwork and data entry.</li></ul> Additional Skills &amp; Qualifications<ul><li>Oncology background preferred, not required.</li><li>Bachelor&#39;s degree preferred, not required (years of experience can compensate).</li></ul> Work EnvironmentThis is a fully onsite opportunity based in Haverford, PA, where you will support a women&#39;s health clinic focused on a breast cancer device trial. Work onsite 5 days per week, ensuring high enrollment in trials. Enjoy 1 week of PTO and 6 holidays as part of our supportive team environment. Job Type &amp; LocationThis is a Contract position based out of Haverford, Pennsylvania.

<h1> Clinical Research Coordinator II</h1> Job DescriptionThe Clinical Research Coordinator plays a crucial role in managing all aspects of clinical research, including patient screening, eligibility assessment, and the coordination of care and follow-up for volunteers involved in research studies, trials, and programs. This role involves recruiting and consenting research participants for various therapeutic areas, providing exceptional service during patient interactions, and coordinating biospecimen collection in collaboration with clinical research nursing staff and laboratory teams. The coordinator ensures ongoing regulatory and protocol compliance through effective collaboration with hospital departments and research teams. Responsibilities<ul><li>Execute and coordinate the informed consent process for research participants across multiple locations, which may involve traveling between sites or using technology.</li><li>Screen patients, assess eligibility, and coordinate the participation and follow-up of volunteers in research studies.</li><li>Recruit and consent research participants for therapeutic areas served.</li><li>Provide concierge-level service for all patient interactions during clinical trials and research studies.</li><li>Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain HIPAA-compliant databases connecting patient information to biospecimens used in research.</li><li>Collaborate with Clinical Research nursing staff, Research Services, laboratory teams, and hospital departments to ensure regulatory and protocol compliance.</li><li>Work with assistant clinical coordinators to ensure compliant data entry 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.</li><li>Maintain sensitivity to cost containment measures while overseeing proposed project budgets from internal and external funding sources.</li></ul>Essential Skills<ul><li>Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks effectively and timely.</li><li>Knowledge of HIPAA data protection and patient advocacy, or similar awareness of ethical treatment of research participants.</li><li>Effective communication skills with research participants, investigators, staff, and external partners.</li><li>Analytical problem-solving skills with sound judgment.</li><li>Adaptability to respond to changing needs in clinical research units.</li><li>Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet use.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor’s degree in Healthcare Administration, Research, or related field with no experience required.</li><li>Associate&#39;s 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>Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for next steps information.

Clinical Research Coordinator II

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator</h1>Job DescriptionThe Research Coordinator will play a vital role in assisting an Investigator, Research Associate, or Project Manager with operationalizing tasks associated with implementing a research study. This role involves a variety of tasks related to recruitment, data collection, data management, and reporting of results. The position offers an opportunity to work in clinical research trials and support one of the leading healthcare providers in the US. Responsibilities<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 via telephone, e-mail, and/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><li>Assist with literature reviews for proposal submissions and manuscript preparation.</li><li>Manage bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.</li><li>Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.</li></ul> Essential Skills<ul><li>Minimum of a high school diploma or General Education Development (GED).</li><li>At least 6 months of clinical research experience.</li><li>Experience in the medical field.</li><li>Experience with phlebotomy and vaccines.</li></ul> Additional Skills &amp; Qualifications<ul><li>Tech savvy.</li><li>Interest in growing within the field of Clinical Research.</li><li>Proficiency in data entry.</li></ul>Work EnvironmentThis position requires working on-site 5 days a week. The role involves supporting clinical research trials within a dynamic and leading healthcare environment. Job Type &amp; LocationThis is a Contract position based out of Raleigh, North Carolina.

Clinical Research Coordinator- Raleigh, NC

<h1 style="font-size: 2em; font-weight: normal;">Clinical Data Coordinator</h1>Job DescriptionJoin a dynamic team dedicated to advancing clinical research by managing and coordinating data for specific disease groups. You will play a crucial role in ensuring data accuracy and compliance, working alongside a data coordinator, clinical coordinator, regulatory coordinator, and nurse. Responsibilities<ul><li>Perform data entry, uploads, and queries with precision.</li><li>Prepare for and assist in audits to ensure compliance.</li><li>Coordinate monitor visits and provide additional support as needed.</li><li>Collaborate effectively within a team divided by disease groups.</li></ul>Essential Skills<ul><li>Proficient in clinical data management with at least one year of experience.</li><li>Experience with EMR systems, ideally EPIC, or similar platforms.</li><li>Ability to resolve data queries and prepare for audits.</li><li>Strong teamwork skills and adaptability to changing priorities.</li></ul>Additional Skills &amp; Qualifications<ul><li>Oncology experience is a plus.</li><li>Certification opportunities with SOCRA or ACRP for career advancement.</li></ul>

Clinical Research Data Coordinator

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Coordinator - Data</h1> Job DescriptionWe are seeking a dedicated Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves coordinating the preparation of study tools, collaborating with research nurses and physicians, and ensuring compliance with protocols. Responsibilities<ul><li>Coordinate the initiation and activation of all new clinical trial protocols.</li><li>Prepare study tools including study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word.</li><li>Review patients&#39; charts and medical history to confirm protocol eligibility and obtain necessary source documents.</li><li>Ensure that IRB approved informed consent forms are obtained, signed, and properly filed.</li><li>Maintain research records for all patients enrolled in studies, including patient consent, eligibility, CRFs, and source documents.</li><li>Assist with grading adverse events using NCI common toxicity criteria and complete SAE forms as required.</li><li>Provide regular reports to tumor study group members and Principal Investigators using Oncore®.</li><li>Serve as a liaison with study sponsors, schedule monitoring visits, and respond to sponsors&#39; queries.</li></ul>Essential Skills<ul><li>Coordinator experience in oncology.</li><li>Registered Nurse (RN) certification.</li><li>Oncology Certified Nurse (OCN) certification.</li><li>Clinical research experience with 1-2 years primarily focused on data entry and query resolution for oncology trials.</li></ul>Additional Skills &amp; Qualifications<ul><li>IATA certification.</li><li>Experience in screening, enrolling, and consenting patients into research studies based on study protocols.</li><li>Experience in medication administration and adverse event reporting.</li><li>Requiring 1-2 years of CRC or data coordinating experience </li></ul> Work EnvironmentThe position is based in an NCI Designated Cancer Center, requiring 1-2 years of CRC experience in oncology. The role involves regular interactions with study sponsors and requires a professional dress code. Job Type &amp; LocationThis is a Contract position based out of Bronx, New York.

<h1>Job Title: Clinical Research Coordinator - Data</h1> Job DescriptionWe are seeking a dedicated Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves coordinating the preparation of study tools, collaborating with research nurses and physicians, and ensuring compliance with protocols. Responsibilities<ul><li>Coordinate the initiation and activation of all new clinical trial protocols.</li><li>Prepare study tools including study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word.</li><li>Review patients&#39; charts and medical history to confirm protocol eligibility and obtain necessary source documents.</li><li>Ensure that IRB approved informed consent forms are obtained, signed, and properly filed.</li><li>Maintain research records for all patients enrolled in studies, including patient consent, eligibility, CRFs, and source documents.</li><li>Assist with grading adverse events using NCI common toxicity criteria and complete SAE forms as required.</li><li>Provide regular reports to tumor study group members and Principal Investigators using Oncore®.</li><li>Serve as a liaison with study sponsors, schedule monitoring visits, and respond to sponsors&#39; queries.</li></ul>Essential Skills<ul><li>Coordinator experience in oncology.</li><li>Clinical research experience with 1-2 years primarily focused on data entry and query resolution for oncology trials.</li></ul>Additional Skills &amp; Qualifications<ul><li>IATA certification.</li><li>Experience in screening, enrolling, and consenting patients into research studies based on study protocols.</li><li>Experience in medication administration and adverse event reporting.</li><li>Requiring 1-2 years of CRC or data coordinating experience</li></ul> Work Environment<ul><li>The position is based in an NCI Designated Cancer Center, requiring 1-2 years of CRC experience in oncology. </li><li>The role involves regular interactions with study sponsors and requires a professional dress code.</li></ul>

SummaryThis role supports participants in a lifestyle-focused clinical study by setting diet and exercise goals, teaching them how to track their progress, and assessing their eligibility based on study criteria. Description- Work with Randomized patients as they receive lifestyle management SOPs at 12 week increments during the study. - Create diet and excursive goals in adherence to the lifestyle protocol of the study. - Teach participants how to capture physical activity and food intake in study provided materials.- In accordance to protocol determine if patients are eligible to participate in the study based on inclusion and exclusion criteria. SkillsNutrition, Health education Top Skills DetailsNutrition, Health education Additional Skills &amp; Qualifications - Need to have an Iowa license	- May need to interact with PI and CRAs occasionally	- GCP certification would be nice, but can be provided Experience LevelIntermediate Level

Clinical Research Dietitian (PT) - IA

SummaryThis role supports participants in a lifestyle-focused clinical study by setting diet and exercise goals, teaching them how to track their progress, and assessing their eligibility based on study criteria. Description- Work with Randomized patients as they receive lifestyle management SOPs at 12 week increments during the study. - Create diet and excursive goals in adherence to the lifestyle protocol of the study. - Teach participants how to capture physical activity and food intake in study provided materials.- In accordance to protocol determine if patients are eligible to participate in the study based on inclusion and exclusion criteria. SkillsNutrition, Health education Top Skills DetailsNutrition, Health education Additional Skills &amp; Qualifications- Need to have an Iowa license	- May need to interact with PI and CRAs occasionally	- GCP certification would be nice, but can be provided Experience LevelIntermediate Level

Clinical Research Dietitian (Part-Time) - IA

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Laboratory Specialist</h1> Job DescriptionWe are seeking a detail-oriented Clinical Research Laboratory Specialist to support the day-to-day research sample collection, processing, storage, and shipment across various clinical trials. This role involves collaborating with coordinators and managers to manage protocols and maintain inventory, contributing significantly to high-profile oncology research projects. Responsibilities<ul><li>Participate in the day-to-day research sample collection, processing, storage, and shipment across clinical trials throughout each protocol’s lifecycle, including start-up, maintenance, and closeout.</li><li>Collaborate with MDG Coordinator and/or Project Manager/Clinical Research Coordinator to review, initiate, and manage protocols requiring the collection and handling of research specimens.</li><li>Assist with maintaining inventory of study-specific materials and supplies.</li><li>Prepare lab kits for various studies.</li><li>Assist with responding to queries and communications with study sponsors.</li></ul>Essential Skills<ul><li>Proficiency in laboratory procedures and biology.</li><li>Strong understanding of quality control and inventory management.</li><li>Experience in oncology and hematology.</li><li>Effective communication skills for data management and patient recruitment.</li><li>Experience in clinical research, including clinical trials and patient record management.</li></ul>Additional Skills &amp; Qualifications<ul><li>Bachelor&#39;s Degree in a Science-related field with 0-1 years of experience or 4+ years of relevant experience without a degree.</li><li>Experience with EDC (Electronic Data Capture) systems and specimen collection.</li></ul>Work EnvironmentThis role operates within a fast-paced environment on a large campus. The work schedule is Monday to Friday, from 11:30 am to 7:00 pm, and requires on-site presence. Benefits include tuition reimbursement upon permanency, excellent health benefits, and opportunities for growth and upward mobility. This position offers the chance to work on high-profile studies with renowned sponsors and gain exposure to groundbreaking oncology research. Job Type &amp; LocationThis is a Contract position based out of Philadelphia, Pennsylvania.

Clinical Research Lab Coordinator

<h1>Clinical Research Nurse</h1> Job DescriptionWe are seeking a highly skilled Clinical Research Nurse to coordinate and oversee clinical operations of clinical trials. This role involves assessing, planning, implementing, and evaluating patient care in clinical research studies. Responsibilities<ul><li>Assist the principal investigator in preparing proposed clinical trials, reviewing trial protocols, and ensuring appropriate departments are notified and equipped.</li><li>Submit protocol revisions, informed consents, continuing reviews, and serious adverse events to the relevant IRB in a timely manner.</li><li>Act as a liaison between principal investigators and sub-investigators on regulatory issues and protocol changes.</li><li>Collaborate with the principal investigator to review studies for feasibility and evaluate potential competition with other protocols.</li><li>Recruit and evaluate study patients, schedule appointments, and conduct interviews.</li><li>Identify the needs of the patient population served, modifying care to meet specific needs.</li><li>Review medical records for potential study patients, ensuring documentation follows protocol guidelines.</li><li>Educate study patients on informed consent procedures, HIPAA authorization, and provide necessary instructions.</li><li>Perform nursing assessments and monitor study patient progress during clinical trials.</li><li>Notify principal investigator of adverse events, including drug toxicity or unexpected side effects, and report serious adverse events to the sponsor and IRB.</li><li>Coordinate research activities, including scheduling laboratory tests and other medical exams.</li><li>Maintain accurate and up-to-date records for each patient participating in clinical trial protocols.</li><li>Prepare for sponsor monitor site visits and ensure all supporting documentation is available.</li></ul>Essential Skills<ul><li>Graduate of a NLN/AACN accredited program in nursing.</li><li>3-5 years of clinical nursing or oncology experience</li><li>Adherence to American Nurses Association standards.</li><li>Mandatory education on human subjects research.</li><li>Clinical Research Experience or Oncology Certified Nurse (OCN).</li></ul>Additional Skills &amp; Qualifications<ul><li>BSN preferred.</li><li>Knowledge of FDA regulatory, IND reporting, and proficiency in Microsoft or similar Office Suite.</li><li>NJ State Professional Registered Nurse License.</li></ul>

Clinical Research Nurse

<h1>Job Title: Clinical Research Nurse</h1> Job DescriptionWe are seeking a dedicated Clinical Research Nurse with extensive experience in oncology to join a prestigious academic research institute. This role is integral in pioneering innovative cancer research and clinical trials aimed at reducing cancer incidence and improving patient outcomes. Responsibilities<ul><li>Coordinate and manage clinical research studies in the field of oncology.</li><li>Interact professionally with physicians and other healthcare professionals to ensure the smooth execution of clinical trials.</li><li>Conduct patient pre-screening and chart reviews to ensure eligibility for study enrollment.</li><li>Manage informed consent processes and maintain compliance with IRB guidelines.</li><li>Report adverse events using CTCAE and ensure patient safety throughout the study.</li><li>Collaborate with research teams to ensure adherence to Good Clinical Practice (GCP) standards.</li></ul>Required Skills &amp; Experience<ul><li>Registered Nurse with a license in the Commonwealth of Pennsylvania.</li><li>At least 5 years of experience as a Registered Nurse with a minimum of 2-3 years in clinical research preferred.</li><li>Extensive experience in oncology, with a focus on hematology and cancer medications.</li><li>Proficiency in adverse event reporting and patient enrollment processes.</li></ul>Please send your resume and 2-3 professional references to hjaquez @actalentservices.com for next steps information.

<h1 style="font-size: 2em; font-weight: normal;">*GREAT OPPORTUNITY TO GET INTO CLINICAL RESEARCH**</h1><h1 style="font-size: 2em; font-weight: normal;">Job Title: Oncology Clinical Research Nurse</h1>Job DescriptionThis role involves overseeing patient visits for phase 1 clinical trials, including taking vitals and collecting specimens to ensure they are delivered to the appropriate lab. You will see 5-7 patients a day across all trials, working collaboratively with your team on various disease groups. Responsibilities are shared among team members, with daily patient visits divided as a team effort. Visit durations range from 1 to 8 hours. You will also perform charting using EPIC, but will not be responsible for data and regulatory work or patient recruitment. Responsibilities<ul><li>Conduct patient visits for phase 1 clinical trials.</li><li>Take vitals and collect specimens during visits.</li><li>Ensure specimens are delivered to the appropriate lab.</li><li>Collaborate with the team to manage workload across all disease groups.</li><li>Perform charting using EPIC.</li></ul>Essential Skills<ul><li>Experience in oncology nursing.</li><li>Proficient in taking patient vitals and blood draws.</li><li>State of Indiana Registered Nursing license.</li></ul>Additional Skills &amp; Qualifications<ul><li>Certified chemotherapy nurse certification is a plus. </li><li>Clinical Research experience is a plus.</li></ul>Work EnvironmentYou will work in a team setting with a schedule of four 10-hour shifts from Monday to Thursday, starting at 7:00 am. There is a mandatory meeting on Friday morning from 8:30 to 9:00 am, with the option to flex time earlier in the week to account for this half-day. Occasionally, you may need to drive to the South Cancer Center to cover patient visits if a team member is unavailable. The organization offers training for oncology nurses in research. Job Type &amp; LocationThis is a 6 month Contract-to-Hire position based out of Indianapolis, Indiana.

Job Title: Clinical Research Nurse (Part-Time – 30 Hours/Week)Contract Duration: 2 MonthsStart Date: November 2025Schedule: Monday through Friday, 30 hours per week during standard business hours<hr><h3>Position Overview:</h3>We are seeking a dedicated and experienced Clinical Research Nurse (CRN) to join our team on a short-term contract basis to support an ongoing vaccine clinical trial. This is an excellent opportunity for a licensed RN to contribute to meaningful work in a collaborative and fast-paced environment. The role is fully onsite and offers a consistent weekday schedule.<hr><h3>Key Responsibilities:</h3><ul><li>Investigational Product (IP) Administration: Safely and accurately administer investigational vaccines in accordance with study protocols and regulatory guidelines.</li></ul><hr><h3>Qualifications:</h3><ul><li>Registered Nurse (RN) License: Active and in good standing.</li><li>Clinical Research Experience: Prior experience in a clinical research setting is preferred.</li><li>IP Administration Experience: Minimum of 1 year administering investigational products in a clinical trial setting.</li><li>Strong Communication Skills: Ability to interact professionally with study participants and team members.</li><li>Attention to Detail: High level of accuracy in documentation and protocol compliance.</li></ul>

<h1>Job Title: Clinical Research Nurse</h1>Job DescriptionWe are seeking a dedicated Clinical Research Nurse to join our team, focusing on the data entry aspects of clinical trials. This role involves documenting adverse events (AEs) and serious adverse events (SAEs), patient-reported outcomes, and engaging with protocol documents. You will handle monitor visits and follow up accordingly. Initially, you will not interact directly with patients, but eventually, you will be responsible for screening and recruiting patients for the trials. Responsibilities<ul><li>Perform data entry for clinical trials.</li><li>Document adverse events (AEs) and serious adverse events (SAEs).</li><li>Manage patient-reported outcomes.</li><li>Review and understand trial protocols.</li><li>Coordinate and follow up on monitor visits.</li><li>Screen and recruit patients for clinical trials (future responsibility).</li></ul> Essential Skills<ul><li>Proficiency in data entry and handling queries.</li><li>Experience with electronic data capture (EDC) systems like Inform and MediData Rave.</li><li>Strong understanding of Good Clinical Practice (GCP) guidelines.</li><li>At least 2 years of nursing experience.</li><li>Knowledge of clinical trial processes at the site level.</li><li>Understanding of IVRS (Interactive Voice Response Systems).</li><li>CITI training certification.</li></ul> Additional Skills &amp; Qualifications<ul><li>Experience in oncology.</li><li>Experience with Epic and clinical research chart review.</li><li>Ability to manage regulatory and IRB-related tasks.</li><li>Adverse event reporting expertise.</li></ul> Work EnvironmentThis role is based at the Farm Journal Building associated with the Abramson Cancer Center. It is a separate entity from the School of Medicine. Job Type &amp; LocationThis is a Contract to Hire position based out of Philadelphia, Pennsylvania.

Clinical Research Nurse Coordinator IIMUST HAVE CLINICAL RESEARCH experience Permanent role with full benefits on day 1Shift: M-F 6:45 am - 3:15 pm  Key Responsibilities:<ul><li>Plan, coordinate, and perform nursing care for research participants </li><li>Execute study protocols and maintain accurate documentation</li><li>Perform physical assessments, phlebotomy, and IV insertions</li><li>Maintain a clean and prepared clinical space</li><li>Review informed consent documents and ensure ongoing patient advocacy</li><li>Manage study records, medications, and test articles securely</li><li>Communicate effectively with investigators, sponsors, and healthcare teams</li><li>Coordinate support staff and ensure adherence to research protocols</li><li>Monitor patient safety and report deviations or concerns to leadership</li></ul>Qualifications:<ul><li>Registered Nurse (RN) with active licensure</li><li>MUST HAVE CLINICAL RESEARCH experience</li><li>Knowledge of FDA regulations, ICH/GCP guidelines, and HIPAA</li><li>Strong interpersonal, organizational, and documentation skills</li><li>Ability to work independently and manage multiple protocols</li><li>Commitment to maintaining a respectful and professional research environment</li></ul>

Job Title: Clinical Research Nurse Pay: $30-38/hr Description:The Research Nurse is responsible for study unit activities in the conduct of Phase 1 clinical trials with emphasis on the safety and welfare of study participants. ·      Enroll patients into clinical trials: Informed Consent (ICF) process- educating, explaining and informing participants of study procedures·      Utilize skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials·      Utilize nursing assessment skills to observe participant general well-being and potential adverse events. ·      Document adverse events and take appropriate action as needed·      Obtain Informed Consent and continue the ICF process by educating, explaining and informing participants of study procedures·      Perform study-related activities such as Cannulation, telemetry, holters, vital signs, ECGs, venipuncture·      Collect and processes biological samples according to the protocol and Standard Operating Procedures·      Record data obtained in a timely, error free manner according to the protocol and Standard Operating Procedures·      Transcribe source data onto the Case Report Form Skills &amp; Qualifications:·      Registered Nurse (RN) - Active and in Good Standing in Texas·      Associates Degree or Bachelors Degree in Nursing (ASN or BSN)·      0-3 Years of nursing experience in a patient facing setting This role has mutliple openings available accross all shifts this includes, 1st shift, 2nd shift, 3rd shift, and rotating. The rotating nurse will be a rotating 3 shifts, with a weekend shift every other week, start times can vary between 1st shift (start time between 5 AM to 7 AM), 2nd shift (start time between 2 PM to 4 PM) and 3rd shift (start time between 10 PM to 12 Midnight). Schedules are typically set 2-3 weeks in advance. Candidates that can accommodate at least one of these shifts can be considered (i.e. only overnights, only evenings, only mornings, only weekends, etc.).

Clinical Research Nurse (Multiple Shifts)

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Clinical Research Nurse - Oncology</h1>Job DescriptionThe Clinical Research Coordinator II RN (CRC-II RN) plays a crucial role within the Research Institute, responsible for planning, coordinating, evaluating, and performing nursing care for research participants. The position involves collecting data for assigned research projects and ensuring adherence to study-specific protocol guidelines, FDA regulations, and ICH/GCP guidelines. The role demands patient advocacy and safe care delivery while maintaining clinical competencies and ensuring a respectful environment for all participants. Responsibilities<ul><li>Plan, coordinate, and evaluate nursing care for research participants in accordance with study protocols.</li><li>Communicate effectively with Principal Investigators, Sub-Investigators, Clinical Research Lead, and support staff.</li><li>Advocate for patient safety and rights, ensuring informed consent and compliance with FDA and ICH/GCP guidelines.</li><li>Maintain clinical competencies, including physical assessment, phlebotomy, and IV insertion.</li><li>Practice Universal Precautions and ensure HIPAA regulations are followed.</li><li>Maintain a clean and prepared clinical space, performing set-up and turnover procedures as needed.</li><li>Participate in training programs to maintain licensure and enhance skills.</li><li>Review informed consent documents with study candidates and ensure ongoing patient advocacy.</li><li>Manage multiple clinical trial protocols, ensuring accurate documentation and confidentiality.</li><li>Promote PI oversight and communicate any deviations or issues affecting trial integrity or participant safety.</li><li>Coordinate support staff and laboratory technicians to ensure efficient and high-quality research outcomes.</li></ul> Essential Skills<ul><li>Experience in clinical research, particularly in oncology and clinical trials.</li><li>Ability to perform chart reviews and pre-screen patients.</li><li>Proficiency in data management and EDC systems.</li></ul> Additional Skills &amp; Qualifications<ul><li>Ability to assist physicians and CRNs with minor procedures.</li><li>Adaptability to integrate into various clinical settings.</li><li>Demonstrated skills in physical assessment, phlebotomy, IV insertion, and drug administration.</li><li>Associate degree in Nursing.</li><li>Minimum 2 years of clinical research experience.</li><li>Active State of FL license as a Registered Nurse.</li><li>BLS certification.</li></ul> Work EnvironmentThis role is based in a hospital environment, requiring interaction with diverse clinical settings and adherence to hospital protocols. Job Type &amp; LocationThis is a Permanent position based out of Altamonte Springs, Florida.

Clinical Research Nurse - Oncology

Clinical Research Nurse Coordinator (RN) – Infusion Experience Required Duties <ul><li>Collaborate with the Principal Investigator (PI) to ensure compliance with FDA regulations, sponsor protocols, and GCP guidelines</li><li>Administer investigational and approved IV therapies</li><li>Screen, recruit, and consent study participants</li><li>Conduct study visits, collect data, and complete case report forms (CRFs)</li><li>Monitor and report adverse events (AEs), serious adverse events (SAEs), and protocol deviations</li><li>Maintain regulatory binders and study documentation</li><li>Manage investigational product inventory and reconciliation</li><li>Coordinate with sponsors during site initiation, monitoring, and close-out visits</li><li>Perform clinical assessments including vital signs, EKGs, and lab specimen collection</li><li>Support onboarding and training of new research staff</li></ul> Qualifications<ul><li>Bachelor’s Degree in Nursing or related field</li><li>Active RN License in the State of Georgia</li><li>Minimum 2 years of clinical research experience preferred</li><li>Infusion experience </li><li>CPR Certification</li><li>IATA Certification (preferred)</li><li>GCP Certification (required)</li><li>Strong knowledge of FDA regulations, GCP, and human subject protection standards</li><li>Excellent organizational and communication skills</li></ul>

Clinical Research Nurse Coordinator

Job Title: Clinical Research Paramedic Pay: $27/hr Description:We are currently seeking a Paramedic, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.) Many are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you´ll be involved with the latest medical technologies and treatments, witnessing their development firsthand.When the drug you worked with gets approved, you know you´ll touch many patient´s lives around the world. <ul><li>Work every other weekend, 12-hr shifts:<ul><li>Rotating to am/pm, 0630-1830; pm/noc, 1830-0630</li><li>Weekend starts on Friday</li><li>Including the Holidays landing on weekends</li></ul></li><li>Available to work all 3 shifts (am/pm/overnight) based on staffing needs</li><li>Available to work additional hours to cover last-minute needs (call-ins).</li></ul> Skills &amp; Qualifications:<ul><li>Completion of Paramedic program and active licensure. </li><li>Current CPR certification</li></ul>

Clinical Research Paramedic

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Recruitment Specialist</h1>Pay: $18 per hourLocation: On-site, Richardson, Texas, 75081Schedule: Tuesday–Saturday, 9:00 AM – 5:30 PMContract Duration: 1–2 years with potential for long-term extensionStart Date: Flexible, ideally the Monday after clearanceBackground Check &amp; Drug Test: Required<h3>About Us</h3>We’re a multinational, multibillion-dollar company specializing in third-party research on consumer products, with a strong focus on the cosmetics industry. We’re expanding our team of Clinical Research Recruiters—individuals who are not only enthusiastic and personable, but also highly proficient in navigating digital systems and tools.<h3>Key Responsibilities</h3><ul><li>Conduct high-volume outbound calls to recruit participants for product testing</li><li>Schedule and coordinate testing appointments</li><li>Maintain accurate records of recruitment activities</li><li>Collaborate with team members to meet daily recruitment goals (approx. 15 participants/day)</li><li>Efficiently manage digital files, folders, and shared documents</li></ul><h3>System &amp; Computer Skills – Required</h3>To ensure fast onboarding and seamless integration, candidates must demonstrate computer competency, including:<ul><li>Navigating SharePoint and Excel spreadsheets with ease</li><li>Locating and organizing files within nested folder structures</li><li>Searching for keywords in PDFs and emails using shortcuts (e.g., Ctrl + F)</li><li>Using keyboard shortcuts like Ctrl + Shift + End, Ctrl + C, Ctrl + V for data handling</li><li>Setting up two-step verification using QR codes and authenticator apps</li><li>Creating and managing browser bookmarks for quick access to key webpages</li></ul><h3>Qualifications</h3><ul><li>Strong communication and interpersonal skills</li><li>Enjoy being on the phone with a “smile and dial” attitude</li><li>Experience in front office, customer service, or medical assistant roles</li><li>Ability to handle high-volume calls and multitask across digital platforms</li><li>Professional, friendly, and tech-confident demeanor</li></ul><h3>Interview Process</h3><ul><li>In-person interview (Monday–Thursday availability)</li><li>Evaluation of system navigation and computer skills may be included</li></ul><h3>Company Culture</h3><ul><li>Friendly, fast-paced, and metrics-driven</li><li>Supportive team environment focused on efficiency and results</li></ul>If you&#39;re someone who thrives in a structured, tech-enabled environment and enjoys connecting with people, we’d love to meet you.

Clinical Research Recruiter

Actalent is looking for a clinical patient recruiter in Richardson, TX! If you are interested in this position, please read over the job description below! Pay: $18/hourSchedule: Monday-Friday 9:00am-5:30pm <h3>Key Responsibilities:</h3><ul><li>Recruit patients for study participation via incoming calls, cold calls, and texting platforms</li><li>Conduct phone screening interviews based on protocol-specific criteria</li><li>Collaborate with Coordinators to meet recruitment goals and assess eligibility</li><li>Schedule screening visits and perform reminder calls</li><li>Maintain accurate recruitment data and update databases</li><li>Follow recruitment policies and procedures for tracking participants</li><li>Implement recruiting strategies and prepare action plans</li><li>Provide weekly updates on recruitment activities</li><li>Maintain an active pipeline of potential participants</li><li>Review and understand assigned study protocols</li><li>Escalate critical findings or trends to the Recruitment Manager</li><li>Support ad hoc projects and other duties as assigned</li></ul><h3>Qualifications:</h3><ul><li>Strong communication and organizational skills</li><li>Experience in patient recruitment or clinical research is a plus</li><li>Ability to work independently and manage multiple tasks</li></ul>If you are interested, please apply today! Two spots available!

Clinical Research Scheduler Needed in Richardson, TX!Great Opportunity to get a foot into Clinical Research Administration!Description:<ul><li>Recruit patients for Clinical Research Studies</li><li>Schedule Patients</li><li>Send cold calls and emails</li><li>Follow up with sourced patients</li><li>Meet productivity goals by sourcing studies to completion</li></ul>Pay: 18.00 USD HourlySchedule: 9:00AM-6:00PM Monday - FridayQualifications:<ul><li>Associates or Bachelors in STEM is a plus</li><li>Call Center Experience is a plus</li></ul>

Clinical Research Scheduler

Clinical Research Study Coordinator

<h1 style="font-size: 2em; font-weight: normal;">Job Title: Research Study Manager</h1>Job DescriptionWe are seeking a dedicated and experienced Research Study Manager to oversee the day-to-day clinical research operations. This role requires a proactive leader with strong experience in oncology and clinical research coordination. Responsibilities<ul><li>Supervise and manage the workflow of coordinators in the assigned disease-specific group.</li><li>Communicate services that will support and enable the growth of clinical research, particularly in recruitment, retention, coordination of research, and data management.</li><li>Conduct quality assurance audits to ensure compliance with regulatory standards.</li><li>Partner with physicians to educate and assist them in selecting appropriate studies and explaining feasibility.</li><li>Work with research sites to oversee oncology research and ensure compliance with protocols.</li><li>Assist doctors in selecting trials and understand screening processes to improve site enrollment.</li></ul>Essential Skills<ul><li>Experience in supervising coordinators and managing workflow.</li><li>Prior experience in oncology and as a Clinical Research Coordinator (CRC).</li><li>Strong understanding of clinical operations and regulatory compliance.</li><li>Bachelor’s Degree in a science discipline.</li><li>3-5 years of oncology experience.</li><li>At least 1 year of supervisory experience.</li></ul>Additional Skills &amp; Qualifications<ul><li>Experience as a Clinical Research Supervisor or Research Program Manager.</li><li>Familiarity with NCI Designated Cancer Institutes.</li></ul>Job Type &amp; LocationThis is a Contract to Hire position based out of New Brunswick, New Jersey.

Clinical Research Study Manager

<h1>Job Title: Clinical Research Technician</h1> Job DescriptionJoin our dynamic team as a Clinical Research Technician!You must be available to work a weekend shift every other week. $23/hr Will work with Clinical Research Nurses and Clinical Research Coordinators to manage Phase I Clinical TrialsTraining will be provided on the first shift for 4-6 weeks to ensure you are well-prepared for the role. You will work with a schedule set 2-3 weeks in advance, ensuring flexibility and planning. Your primary role will be collaborating with Clinical Research Nurses and Coordinators to manage Phase I Clinical Trials. Responsibilities<ul><li>Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.</li><li>Prepare and accurately record ECGs/Holters.</li><li>Collect and process biological samples as specified in the protocol, ensuring proper distribution.</li><li>Monitor meals to ensure dietary compliance by research participants.</li><li>Assist in the preparation of rooms and medical equipment.</li><li>Assist with screening procedures as needed.</li><li>Maintain a clean, safe, and efficient working and study environment.</li><li>Build respectful relationships with study participants.</li><li>Accurately record all research data obtained or observed.</li><li>Assist with quality control of source documents and case report forms.</li><li>Maintain a basic understanding of current regulatory requirements.</li><li>Attend all required meetings, as appropriate.</li><li>Assist as necessary with study procedures.</li><li>Maintain accurate records of all work undertaken.</li><li>Maintain skills to perform all study tasks, as required.</li><li>Maintain constant awareness of participant safety and dignity at all times.</li><li>Handle participant complaints efficiently and effectively to maintain satisfaction.</li><li>Ensure client and participant confidentiality is maintained.</li><li>Respond to client and team queries in a timely manner.</li><li>Take ownership for the quality and standard of your work.</li></ul>Essential Skills<ul><li>Patient Care</li><li>Laboratory skills</li><li>Clinical Research</li><li>EKG proficiency</li><li>Clinical Trial experience</li><li>Sample preparation</li><li>Phlebotomy</li><li>Chart review</li><li>Knowledge of Biology</li><li>Healthcare proficiency</li><li>Understanding of FDA, ICH, and GCP guidelines</li></ul>Additional Skills &amp; Qualifications<ul><li>High School Diploma, CNA, Medical Assistant, EMT, or a Bachelor&#39;s Degree in Science/Healthcare</li><li>0-2 years of experience in science, healthcare, or research</li><li>Phlebotomy skills are nice to have</li></ul>

Clinical Research Technician

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