• Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated trials. Research coordinator work includes study design, protocol ... to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. This position is responsible for study… more
    University of Pennsylvania (10/07/25)
    - Related Jobs
  • Sr. Director Research - Administration - Full Time

    Guthrie (Sayre, PA)
    …expenses. + Manage pharmaceutical and federally funded study contracts, billing compliance , and audit preparation. + Maintain dashboards to monitor ... a senior administrative executive to collaboratively lead the strategic, operational, and compliance functions of DGF. This role is central to ensuring the effective… more
    Guthrie (08/13/25)
    - Related Jobs
  • Clinical Research Coordinator A/B/C

    University of Pennsylvania (Philadelphia, PA)
    …wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Research ... to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. Our projects occur throughout the Department… more
    University of Pennsylvania (10/02/25)
    - Related Jobs
  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …manuscripts, grant proposals, and presentations. Works closely with the Principal Investigator , manager, and study team to address study needs, implement approved ... changes, and monitor outcomes. Contributes to investigator -initiated, multi-center, and patient-oriented clinical and translational research studies. Job Description… more
    University of Pennsylvania (10/08/25)
    - Related Jobs
  • Associate Director Oncology Research Operations…

    Penn Medicine (West Chester, PA)
    …with major internal (PI, Regulatory, Legal, Budget, Finance, Billing Compliance , Infusion, Pharmacy) and external (sponsors, facilities, CROs, Subcontractors, ... including blood, urine and tissue samples, participate in initiation, monitoring, audit and close-out visits, coordinate study team meetings, disease site and/or… more
    Penn Medicine (10/14/25)
    - Related Jobs
  • Asset Protection - Agent - East Coast Fulfillment…

    Nordstrom (Elizabethtown, PA)
    …of shrinkage/loss and follow through on resolutions in partnership with Investigator and/or Asset Protection Manager. + Maintain all site-required documentation ... issues (ie accident reports, inspection reports, training logs etc.) + Audit physical security infrastructure (ie intrusion detection, access control, cameras) and… more
    Nordstrom (10/14/25)
    - Related Jobs
  • Research Coordinator - Heart Vascular Research…

    WellSpan Health (York, PA)
    …and some evenings **General Summary** Coordinates clinical research activities and compliance to study requirements, and patient and staff considerations relative to ... study requirements. + Assists investigators in evaluating the quality of care and compliance to protocol requirements. Follows by ensuring compliance with all… more
    WellSpan Health (07/22/25)
    - Related Jobs
  • Clinical Research Coordinator A

    University of Pennsylvania (Philadelphia, PA)
    …Studies Unit (CSU). The CRC will coordinate and implement investigator -initiated, industry-sponsored, and translational studies (Phase II-IV) across a diverse ... files and data entry in REDCap and other databases; support monitoring and audit activities. + Collaborate with investigators and staff; contribute to team meetings.… more
    University of Pennsylvania (09/19/25)
    - Related Jobs
  • Clinical Research Nurse

    Vitalief (Philadelphia, PA)
    …clinical research studies, including NIH-sponsored, industry-sponsored, and investigator -initiated trials. + Work independently managing day-to-day research ... ensure accurate data collection/entry. + Manage regulatory binders, IRB submissions, and compliance with FDA, IRB, and GCP guidelines. + Monitor safety events,… more
    Vitalief (09/18/25)
    - Related Jobs
  • Clinical Research Coordinator

    Vitalief (Philadelphia, PA)
    …clinical research studies, including NIH-sponsored, industry-sponsored, and investigator -initiated trials. + Work independently managing day-to-day research ... ensure accurate data collection/entry. + Manage regulatory binders, IRB submissions, and compliance with FDA, IRB, and GCP guidelines. + Monitor safety events,… more
    Vitalief (09/18/25)
    - Related Jobs