Clinical Research Associate jobs in Virginia

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Clinical Research Coordinator
  • Clinical Research Partners
  • Richmond, VA FULL_TIME
  • Job Description

    Responsibilities and Duties

    Under direct supervision of Principal Investigator and Team Leader of Research and recruitment/Lead Clinical Research Coordinator, the Clinical Research Coordinator will

    • Complete training requirements such as IATA/HAZMAT, sponsor specific training modules, GCP and eCRF training courses.
    • Conduct/monitor the screening and recruitment of subjects for research trials using knowledge of current protocols and inclusion/exclusion criteria to determine subject eligibility.
    • Explain informed consent specific to protocol to potential enrollees, answers questions if any, and documents the informed consent process.
    • Educate subjects on protocol related procedures/assessments in which they must participate as a study subject.
    • Collect, organize, and maintain data and test results for source documentation of all research subjects.
    • Assist in the management of the study subjects' health status during the course of research care and development of treatment plan related to the research protocol. Conduct any needed assessments using protocols for review by the PI when appropriate.
    • Completes visit procedures according to protocol schedule and checks on visit measurements, lab results, concomitant medications and presence of adverse events.
    • Draw blood when needed, process and ships specimen according to sponsor requirements including vital signs, EKG and radial augmentation index studies.
    • Complete source documents and enters the same in the CRF or eCRF.
    • Work closely with sponsor monitors during site initiation visits, site monitoring visits, and answer queries when needed.
    • Complete drug accountability records, dispense study medications per protocol requirements or through the IVRS.
    • Miscellaneous duties such as keeping records of temperature logs of drugs storage and freezers.
    • Complete study close out visit by proper drug accountability and shipment of used and unused study medications.
    • Responsible for IRB submissions, SAE reporting, continuing approval reports.
    • Maintain Trial Master Files & document according to Regulatory Retention Requirements. - Document all of the above in a timely manner.
    • Knowledge, Skills, and Abilities: Work requires the ability to understand and follow oral and written instructions generally acquired through a high school education and medical assistant programming.
    • Sources viable subjects and pre-screens candidates to determine a fit for current study needs.
    • Conduct chart reviews and contact subjects for screening visits.
    • Have knowledge of all the active studies at CRP. - Take in coming calls from Radio Ads and TV ads and schedule prescreening/ screening visits.
    • Create prescreening form to complete for when radio ad or TV ad runs to go over study with the subjects.
    • On days when no patients are being seen by CRC 10 recruitment calls are expected to be made.
    • All recruitment attempts/ calls are to be completed on the communication log and turned into the Lead CRC daily.
    • Maintain and organize all study supplies. (putting away lab kits, IP, study binders and any other study supplies.)

    Qualifications And Skills

    High School Diploma or GED equivalent. Certificate from accredited Medical Assistant Program or higher. Clinical research certification (ACRP, SoCra) is a plus.

    Job Type: Full-time
  • 11 Days Ago

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Clinical Research Quality Assurance
  • Clinical Research Partners
  • Richmond, VA FULL_TIME
  • Job DescriptionThe QAS position is responsible for the execution of the Quality Assurance (QA) audit activities on assigned studies/products/vendors. This role is accountable for Good Clinical Practic...
  • 11 Days Ago

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Clinical Research Patient Recruiter
  • Alcanza Clinical Research
  • Charlottesville, VA FULL_TIME
  • Department: Patient RecruitmentEmployment Type: Full TimeLocation: Charlottesville Medical Research Center | Charlottesville, VAReporting To: Jade ClarkDescriptionAlcanza is a growing multi-site, mult...
  • 12 Days Ago

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Medical Assistant / Lab Tech / Clinical Research Assistant
  • Alcanza Clinical Research
  • Charlottesville, VA FULL_TIME
  • Medical Assistant / Lab Tech / Clinical Research AssistantDepartment: Operations Employment Type: Full TimeLocation: Charlottesville Medical Research Center | Charlottesville, VAReporting To: Caryn Gi...
  • 2 Months Ago

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Senior Clinical Research Coordinator
  • Tekton Research
  • Burke, VA FULL_TIME
  • Tekton Research is seeking an Experienced Clinical Research Coordinator to join our team in Burke, VA.This is an onsite position located at: 8988 Fern Park, Burke, Virginia 22015Responsibilities inclu...
  • Just Posted

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Clinical Research Associate
  • LifeNet Health
  • Virginia, VA FULL_TIME
  • Clinical Research Associate Location: Virginia Beach, VA Department: Global Clinical Affairs Job Type: Full-Time Shift: Monday-Friday 8:15AM-5:00PM; Other times as assigned/up to 75% travel with overn...
  • 4 Days Ago

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Clinical Research Associate
  • McInnis Inc.
  • Ridgefield, CT
  • The Clinical Research Associate will support clinical research activities within research sites that are actively partic...
  • 6/12/2024 12:00:00 AM

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Clinical Research Associate
  • Insight Global
  • Day to Day: Coordinate all front office functions, including addressing customer's needs organizing workflow, making adj...
  • 6/12/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

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Clinical Research Associate
  • Advarra
  • About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
  • 6/11/2024 12:00:00 AM

Virginia (/vərˈdʒɪniə/ (listen)), officially the Commonwealth of Virginia, is a state in the Southeastern and Mid-Atlantic regions of the United States located between the Atlantic Coast and the Appalachian Mountains. Virginia is nicknamed the "Old Dominion" due to its status as the first English colonial possession established in mainland North America and "Mother of Presidents" because eight U.S. presidents were born there, more than any other state. The geography and climate of the Commonwealth are shaped by the Blue Ridge Mountains and the Chesapeake Bay, which provide habitat for much of ...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Associate jobs
$68,874 to $90,972

Clinical Research Associate in Vista, CA
Represents Global Clinical Affairs on multifunctional teams tasked with preparing responses to regulatory agencies.
May 02, 2023
Clinical Research Associate in Stockton, CA
Document informed consent discussion and obtain signatures per protocol, federal, state and institutional requirements.
April 20, 2023
Clinical Research Associate in Stamford, CT
Responds flexibly to changing business demands and opportunities, proactively looking for ways to contribute.
May 09, 2023
Participate in monitoring visit report review process in order to maintain oversight of clinical monitoring quality and adherence to protocol and established processes and plans.
December 03, 2022