• Trial Master File

    Sumitomo Pharma (Trenton, NJ)
    …information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File ( TMF ) Specialist will be ... for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits...overall quality, maintenance, and completeness of Trial Master Files. + Working closely with the TMF more
    Sumitomo Pharma (11/05/25)
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  • Senior Manager Clinical Study Lead (Cell Therapy)

    Regeneron Pharmaceuticals (Warren, NJ)
    …of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File ( TMF ) etc. + Ensures compliance with the ... limited to database lock, reconciliation of vendor contracts, budget, TMF , and study drug accountability + Contributes to clinical...masked investigational product, set up and management of unmasked trial master file , review of… more
    Regeneron Pharmaceuticals (10/10/25)
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  • CRA 2, Early Clinical Development, IQVIA Biotech

    IQVIA (New York, NY)
    …of data queries. + Ensure that essential documents are collected and maintained in both the Trial Master File ( TMF ) and the Investigator Site File ... (ISF) in accordance with regulatory standards. + Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence. + Work closely with cross-functional project teams to support study execution and ensure… more
    IQVIA (11/01/25)
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  • Clinical Supplies Associate

    System One (Basking Ridge, NJ)
    …activities, including product destruction, study close-out, and filing documents in the electronic Trial Master File (e- TMF ). Requirements: + Background ... Pay: $30-34/hour Responsibilities: + Monitor and assess temperature data for clinical trial shipments and on-site storage. + Collaborate with Quality to evaluate… more
    System One (10/18/25)
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  • Sr. Study Manager, Clinical Operations

    Taiho Oncology (Princeton, NJ)
    trial completion. + Overall responsible for the Trial Master File , including review of the TMF plan, related metrics, and ongoing quality review of ... or multiple global trials by managing all aspects of trial deliverables, including development of timelines, budget, recruitment and...the TMF . Oversee TMF related CRO and internal… more
    Taiho Oncology (11/13/25)
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  • Study Associate I, Clinical Operations

    Taiho Oncology (Princeton, NJ)
    …ensure consistency across studies and alignment with internal TMF procedures. + Monitors Trial Master File related KPIs and performs quality review of ... updating of study trackers and systems and overseeing study documentation and Trial Master File . The SA supports the Clinical Operations department with… more
    Taiho Oncology (11/13/25)
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