• TMF Specialist

    Actalent (Philadelphia, PA)
    Job Title: TMF SpecialistJob Description The TMF Specialist serves as the subject matter expert for all aspects of the Trial Master File ( TMF ). This role ... compliance with regulatory standards. Responsibilities + Act as the TMF expert for all studies and provide guidance on...or similar eTMF platforms. + Manage user access to TMF binders and perform quality control of filed documents.… more
    Actalent (12/02/25)
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  • Trial Master File ( TMF ) Specialist…

    Sumitomo Pharma (St. Paul, MN)
    …website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File ( TMF ) Specialist will be responsible for ensuring that SMPA studies ... inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable functions follow the requirements of the TMF… more
    Sumitomo Pharma (11/05/25)
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  • TMF Specialist / Clinical Trial…

    Actalent (Durham, NC)
    Job Title: TMF Specialist Job Description To maintain continuity and compliance across ongoing medical device trials, we are seeking a TMF Specialist to ... Responsibilities * Maintain and oversee the Trial Master File ( TMF ) for active medical device studies, ensuring completeness, accuracy,...* Serve as the central point of contact for TMF related queries between sponsors, CROs, sites, and regulatory… more
    Actalent (12/02/25)
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  • Regulatory Specialist C

    University of Pennsylvania (Philadelphia, PA)
    …as well as organize and maintain all regulatory affairs documentation/Trial Master files ( TMF ) as required. The Regulatory Affairs Specialist C is expected to ... organize and maintain all regulatory affairs documentation/Trial Master files ( TMF ) as required. The Regulatory Affairs Specialist ...files ( TMF ) as required. The Regulatory Affairs Specialist C is expected to resolve regulatory and data… more
    University of Pennsylvania (10/09/25)
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  • Site Specialist II

    ICON Clinical Research (Blue Bell, PA)
    Site Specialist II - Remote - US ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive ... future of clinical development. ICON is hiring for Site Specialist II and Sr. Site Specialist **Title:**...Ensure accuracy and timely completeness of Trial Master File ( TMF ) documents submitted during start-up and perform a Quality… more
    ICON Clinical Research (11/21/25)
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  • Clinical Study Specialist (Office-based…

    ICON Clinical Research (NJ)
    Clinical Study Specialist (office based) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive ... + Performs scheduled reconciliations of study Trial Master File ( TMF ) with clinical study lead guidance + Ensures scheduled...(NA, LAM, EU, APAC, India) + Experience working in TMF , CTMS, Sharepoint, + Excels in written and verbal… more
    ICON Clinical Research (12/02/25)
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  • Manager Medical Staff Services

    Texas Health Resources (Bedford, TX)
    …health professionals. 2. Advise the Medical Staff Coordinator and Credentialing Specialist regarding difficult privileging issues. 3. Responsible for complete and ... the maintenance of same through the Medical Staff Coordinator and Credentialing Specialist . 4. Responsible for timely notification to all applicants of the granting,… more
    Texas Health Resources (11/04/25)
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