• Trial Master File…

    Sumitomo Pharma (Phoenix, AZ)
    …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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  • CRA 2, Oncology, Full Service, IQVIA

    IQVIA (Glendale, AZ)
    …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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  • Clinical Research Associate (CRA)

    Vitalief (Phoenix, AZ)
    …to ensure alignment with study timelines and quality expectations. + Review and maintain Trial Master File ( TMF ) content for accuracy, timeliness, ... Development, Regulatory, Data Management, Safety, and Quality teams to ensure seamless trial execution. + Support audit and inspection readiness efforts and assist… more
    Vitalief (10/16/25)
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  • CRA 2, Early Clinical Development, IQVIA Biotech

    IQVIA (Glendale, AZ)
    …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 (09/10/25)
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