• BeOne Medicines (San Mateo, CA)
    …Responsible for working with regional and country teams to ensure that country and site level Trial Master File is created, maintained and QC'd on a regular ... clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for...basis as per the study TMF QC plan + Provides input to Global Clinical… more
    DirectEmployers Association (10/29/25)
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  • Trial Master File

    Sumitomo Pharma (Sacramento, CA)
    …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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  • Clinical Research Associate, Sponsor Dedicated

    IQVIA (Carlsbad, CA)
    …phase. * Ensure copies/originals (as required) site documents are available for filing in the Trial Master File ( TMF ) and verify that the Investigator's ... be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications *… more
    IQVIA (11/12/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    …Support start-up phases as required. Documentation: Ensure all site documents are filed in the Trial Master File ( TMF ) and Investigator's Site File ... Associate! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and sponsor… more
    IQVIA (11/06/25)
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  • Sr. CRA, Sponsor Aligned, Oncology

    IQVIA (Carlsbad, CA)
    …start-up phase. + Document Management: Ensure site documents are available for filing in the Trial Master File ( TMF ) and verify that the Investigator's ... Management: If applicable, manage site financials according to the clinical trial agreement and retrieve invoices as required by local regulations.… more
    IQVIA (11/05/25)
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  • CRA 2, Oncology, Full Service, IQVIA

    IQVIA (San Francisco, CA)
    …start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File ( TMF ) and verify that the ... be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Education:… more
    IQVIA (10/22/25)
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  • CRA 2, Early Clinical Development, IQVIA Biotech

    IQVIA (San Francisco, CA)
    …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 (09/04/25)
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  • Sr Manager, Supply Chain

    Gilead Sciences, Inc. (Foster City, CA)
    …+ Maintains compliance of clinical supply deliverables for clinical study reports (CSR) and trial master file ( TMF ). + Maintains compliance with ... ERP system. Has good understanding and working knowledge in master data management. + Data and analytics: oversees the...Doctorate and 2+ years of Industry experience OR + Master 's and 6+ years of Industry experience OR +… more
    Gilead Sciences, Inc. (09/09/25)
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  • Clinical Trial Associate, Selution (Onsite…

    Cordis (Irvine, CA)
    …study tasks from start-up phase through study completion + Maintain internal Trial Master Files (TMFs) and prepare study TMF for audit readiness + Assist in ... that address unmet and critical medical needs. **Responsibilities** We are seeking a Clinical Trial Associate in Irvine, CA to join our clinical study team in the… more
    Cordis (10/29/25)
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