• Clinical Research Coordinator -…

    Virtua Health (Marlton, NJ)
    …as required by protocol to ensure the submission of accurate information to clinical trial sponsors and regulatory agencies.* Responsible for submitting all ... Health System - 1600 Haddon Ave Job Information: *This is not a remote position* Summary:Coordinates and participates in clinical research studies conducted by… more
    Virtua Health (08/22/24)
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  • Clinical Research Coordinator Multi…

    Virtua Health (Marlton, NJ)
    …which may include quality improvement data and tracking information submitted to clinical trial sponsors and regulatory agencies. Coordinates visits for ... Additional Locations: Job Information: Job Summary: Coordinates and participates in clinical research studies conducted by principal investigators. Acts as a liaison… more
    Virtua Health (09/12/24)
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  • Clinical Research Coordinator A/B…

    University of Pennsylvania (Philadelphia, PA)
    …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A/B - PEACE Family Planning (OBGYN) Job Profile ... Title Clinical Research Coordinator A Job Description Summary...overall study management of participants. Intercept and respond to trial participant phone calls. Perform telephone follow-up as per… more
    University of Pennsylvania (09/08/24)
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  • Immunotherapy Nurse Coordinator

    University of Pennsylvania (Philadelphia, PA)
    …to establish a nursing plan of care and provide exemplary patient care to clinical trial patients. + Administer study drug medications and other treatment ... resources, and much more. Posted Job Title Immunotherapy Nurse Coordinator Job Profile Title Veterinary Technician D Job Description... trials in- and outpatients as needed. + Support clinical trial protocol implementation, data collection and… more
    University of Pennsylvania (08/21/24)
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  • Sr Clinical Research Associate

    J&J Family of Companies (Trenton, NJ)
    …of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation ... parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols,...* Clinical research certification (ACRP or SoCRA, Clinical Coordinator /CRA certification) preferred. * Ability to… more
    J&J Family of Companies (09/06/24)
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