• TMF Specialist / Clinical…

    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 ... integrity of trial documentation. Responsibilities * Maintain and oversee the Trial Master File ( TMF ) for active medical device studies, ensuring… more
    Actalent (12/02/25)
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  • Trial Master File ( TMF…

    Sumitomo Pharma (St. Paul, MN)
    …on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File ( TMF ) Specialist will be responsible for ... for audits and inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable...Trial Master Files. + Working closely with the TMF Process Owner, identify trends or quality concerns and… more
    Sumitomo Pharma (11/05/25)
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  • 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 ... compliance with regulatory standards. Responsibilities + Act as the TMF expert for all studies and provide guidance on...other eTMF platforms. + Proficiency in document management and clinical trial inspection readiness. Additional Skills &… more
    Actalent (12/02/25)
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  • Clinical Study Specialist…

    ICON Clinical Research (NJ)
    … clinical trial registry postings + Performs scheduled reconciliations of study Trial Master File ( TMF ) with clinical study lead guidance + Ensures ... Clinical Study Specialist (office based) ICON... Clinical Study Specialist (office based) ICON plc is a world-leading...(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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  • Regulatory Specialist C

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

    ICON Clinical Research (Blue Bell, PA)
    …and we welcome you to join us on our mission to shape the future of clinical development. ICON is hiring for Site Specialist II and Sr. Site Specialist ... Site Specialist II - Remote - US ICON plc...action planning. + Ensure accuracy and timely completeness of Trial Master File ( TMF ) documents submitted during… more
    ICON Clinical Research (11/21/25)
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