• 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 Study Lead

    Actalent (South San Francisco, CA)
    …members on study protocol and trial conduct processes + Ensure that the Trial Master File ( TMF ) is set up and maintained appropriately throughout the ... trial and conduct periodic TMF reviews/QCs, as needed + Ensure the clinical trial (s) are inspection ready at all times and participate in Quality Assurance… more
    Actalent (11/14/25)
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  • Study Start Up Associate II - Oncology

    ICON Clinical Research (San Diego, CA)
    …and escalate issues as soon as identified. + Ensure accuracy and timely completeness of Trial Master File ( TMF ) documents submitted during start-up and ... (SIS) and Informed Consent Forms (ICF): + Prepare, review and approve Global Master ICF templates for Sponsors. + Prepare, review and approve Country Master more
    ICON Clinical Research (11/21/25)
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  • Clinical Research Associate II/Sr. Clinical…

    Parexel (Sacramento, CA)
    …documentation, updates and tracking within required timeframes, including but not limited to Trial Master File ( TMF ) documentation, site reports, ... with the set-up, running and close-out of sites in a clinical trial . **Monitoring Responsibilities and Study Conduct:** + Ensure proper conduct of clinical… more
    Parexel (11/22/25)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …planning, designing case report forms (CRFs), and training of study sites. + Maintain and audit Trial Master File ( TMF ) and upload to eTMF to ensure ... Opportunity** The CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to… more
    Abbott (11/18/25)
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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 (11/18/25)
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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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  • 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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  • 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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