• 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 (Heme/Onc)

    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 (10/29/25)
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  • Clinical Study Specialist (Office-based - Warren,…

    ICON Clinical Research (NJ)
    …supports with clinical trial registry postings + Performs scheduled reconciliations of study Trial Master File ( TMF ) with clinical study lead ... supporting global trials (NA, LAM, EU, APAC, India) + Experience working in TMF , CTMS, Sharepoint, + Excels in written and verbal communications + Self-starter, can… more
    ICON Clinical Research (10/18/25)
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  • Clinical Research Associate - Sponsor Dedicated

    IQVIA (Parsippany, NJ)
    …phase. * Ensure copies/originals (as required) site documents are available for filing in the Trial Master File ( TMF ) verify that the Investigator's Site ... be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications *… more
    IQVIA (10/18/25)
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  • CRA 2, Car-T, Iqvia Biotech

    IQVIA (Parsippany, NJ)
    …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 (10/02/25)
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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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