• Clinical Research Coordinator B/C (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …performed, reporting adverse events and ensuring review and appropriate follow-up by investigator , monitoring patient care and treatment side effects in concert with ... with design, set-up and execute studies. Be responsible for writing investigator -initiated IND/IDE clinical trials in collaboration with faculty supervisor. Speak at… more
    University of Pennsylvania (05/04/25)
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  • Clinical Research Coordinator B/C (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …requirements, and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report ... contribute to study-related meetings, including but not limited to Investigator Meetings, Site Initiation Visits, Intermediate Monitoring Visits, Close-out Visits,… more
    University of Pennsylvania (05/04/25)
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  • Clinical Research Coordinator 2

    Stanford University (Stanford, CA)
    …we encourage you to apply! The CRC2 will work closely with the Investigator (s) and Clinical Research Manager (CRM) in a dynamic environment, and be responsible ... strategies, oversee study operation and conduct, oversee regulatory compliance and financial logistics, and ensure overall progress on projects. The position will… more
    Stanford University (04/26/25)
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  • Clinical Research Coordinator II

    Geisinger (Danville, PA)
    …study protocols. + Administers and monitors study drug as directed by the investigator and clinician. + Performs triage nursing assessments of subjects as needed. + ... protocols. + Monitors lab results and reports all findings to the principal investigator . + Informs principal investigator of all relevant patient care issues… more
    Geisinger (04/18/25)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    …accordance with study protocol, coordinating these visits with the Principal Investigator . + Develops, implements, and evaluates subject recruitment and retention ... accordance with study protocol, coordinating these visits with the Principal Investigator . + Resolves questions and concerns received from study subjects, triaging… more
    University of Rochester (04/02/25)
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  • Clinical Trials Coordinator - Urology

    UCLA Health (Los Angeles, CA)
    …multicenter clinical trials (both NIH and industry-sponsored), local investigator -initiated clinical trials, and/or programmatic clinical research activities. Duties ... Good Clinical Practice (GCP). + Collaborating with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors,… more
    UCLA Health (05/23/25)
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  • Sr. Grants & Contracts Analyst

    Johns Hopkins University (Baltimore, MD)
    …guidance on protocols, regulations, and guidelines to the Principal Investigator (PI), research staff, and other scientific/research professionals, both within ... may involve highly detailed budgets, multiple projects, Cores and Subawards, Investigator -initiated, Consortium, and New Center Dept. of Defense grants, higher… more
    Johns Hopkins University (05/22/25)
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  • Research Assistant-Clinical

    Arkansas Children's (Little Rock, AR)
    …projects, supervised by the Clinical Research Supervisor and Principal Investigator . Responsibilities include meticulous adherence to study protocols, managing data ... as the primary administrative liaison between study participant and Principal Investigator or other research staff. Coordinates project activities, scheduling, and… more
    Arkansas Children's (05/04/25)
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  • Clinical Research Manager - Cutaneous Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Trials Office. The Clinical Research Manager, in collaboration ... protocol and regulatory compliance, patient safety, staff development & training and financial goals, as defined by Senior Research Leadership and the DFCI Clinical… more
    Dana-Farber Cancer Institute (05/03/25)
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  • Director of Clinical Research Consulting

    Vitalief (New Brunswick, NJ)
    …develop, direct and manage the execution of the strategic, operational and financial delivery of required Clinical Trials Study Activation activities. + Perform the ... follow through to approval; Final Preparation - Final approvals by the Principal Investigator & Sponsor. + Take a lead role in developing long-standing relationships… more
    Vitalief (05/01/25)
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