• Clinical Research Coordinator A/B/C

    University of Pennsylvania (Philadelphia, PA)
    …A high degree of autonomy, leadership, and expertise in GCP and institutional policies is expected. QUALIFICATIONS: Clinical Research Coordinator A* Bachelor's ... research ethics and an interest in learning about IRB processes and human subject research regulations...disability, veteran status or any class protected under applicable federal , state or local law . Special Requirements Background… more
    University of Pennsylvania (09/19/25)
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  • Clinical Research Coordinator II

    Dana-Farber Cancer Institute (Foxborough, MA)
    …as required. Maintains site regulatory binders and ensures study compliance with all state, federal , and IRB requirements. May be responsible for site IRB ... The Clinical Research Coordinator work within the Dana-Farber Regional Campus...site(s). + Prepare and/or complete regulatory related reports and IRB submissions as it pertains to the regional campus'… more
    Dana-Farber Cancer Institute (08/28/25)
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  • Research Program Coordinator - Medicine…

    Mount Sinai Health System (New York, NY)
    …submission, and maintenance of regulatory documentation in accordance with institutional , federal , and international guidelines. The coordinator will ... multi-site clinical trials, including domestic and international locations. + Prepare, review , and submit regulatory documents (eg, IRB /IEC submissions, informed… more
    Mount Sinai Health System (10/11/25)
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  • Clinical Research Coordinator - Center…

    Dana-Farber Cancer Institute (Boston, MA)
    …Responsible for maintaining regulatory binders and assuring study compliance with all state, federal , and IRB mandates. This individual will also register study ... the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. +… more
    Dana-Farber Cancer Institute (11/11/25)
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  • Sports Clinical Research Coordinator

    University of Utah (Salt Lake City, UT)
    …set by governing agencies. Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures; and the ability to ... the study. 7. Represents the research program at meetings, national and international research consortia. 8. Prepares, submits and maintains IRB , FDA , NCI… more
    University of Utah (11/04/25)
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  • Sr. Research Nurse (Oncology) - #Staff

    Johns Hopkins University (Baltimore, MD)
    …required regulatory documents. + May participate in drug data sheet development/ review /revision. + Monitors for IRB approval/request for further information ... Senior Division Manager, Nurse Manager and or the Lead Research Nurse, we are seeking a **_Sr Research...design to evaluate new protocol.s + Applies knowledge of federal & local regulations when evaluating new protocols. +… more
    Johns Hopkins University (11/04/25)
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  • Research Coordinator

    University of Utah (Salt Lake City, UT)
    …with guidelines set by governing agencies. Assists and supports PI and other research staff with literature reviews, document review and editing, qualitative ... Rate Range** 31600 to 50000 **Close Date** 11/30/2025 **Priority Review Date (Note - Posting may close at any... research program at meetings, national and international research consortia. 6. Prepares, submits and maintains IRB more
    University of Utah (10/31/25)
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  • Clinical Research Coordinator III

    Rush University Medical Center (Chicago, IL)
    …procedural documentation in compliance with institutional , local, state, and federal guidelines and regulations related to clinical research . 5. Oversees ... Professionals (CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) **Job… more
    Rush University Medical Center (10/23/25)
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  • Clinical Research Associate I

    Stony Brook University (Stony Brook, NY)
    …duties: + Review all active protocols, manage clinical trials from IRB initiation to close-out. + Sponsor's monitoring visits, and responsible for drug/device ... Clinical Research Associate I **Required Qualifications (as evidenced by...+ Submit pharmaceutical proposals and consent forms to the IRB . + Liaison between SBMC, pharmaceutical sponsor, patient and… more
    Stony Brook University (10/18/25)
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  • PS Clinical Research Coord

    University of Utah (Salt Lake City, UT)
    …the study. 6. Represents the research program at meetings, national and international research consortia. 7. Prepares, submits and maintains IRB , FDA , NCI ... Rate Range** 39300 to 72700 **Close Date** 01/14/2026 **Priority Review Date (Note - Posting may close at any...Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more
    University of Utah (10/15/25)
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