• Trial Master File…

    Sumitomo Pharma (Topeka, KS)
    …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 Clinical Research Associate - FSP

    Parexel (Topeka, KS)
    …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 (11/20/25)
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  • Clinical Research Associate - Sponsor Dedicated

    IQVIA (Overland Park, KS)
    …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 (Overland Park, KS)
    …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 (Lenexa, KS)
    …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 (Overland Park, KS)
    …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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