• Senior Manager, Biostatistics

    Edwards Lifesciences (Nashville, TN)
    …the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience + The ... + Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global ...trials with skill levels exceeding the requirements of the Associate Manager Required or + Master's Degree or equivalent… more
    Edwards Lifesciences (07/11/24)
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  • Sr Clinical Research Associate

    J&J Family of Companies (Nashville, TN)
    …of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation ... Sr Clinical Research Associate - 2406209639W **Description**...parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols,… more
    J&J Family of Companies (09/06/24)
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  • Sr Clinical Research Associate

    ThermoFisher Scientific (Nashville, TN)
    clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... required. Ensures study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC check of reports generated from… more
    ThermoFisher Scientific (09/15/24)
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  • CRA II

    ICON Clinical Research (Brentwood, TN)
    …as a Clinical Research Associate . + In-depth kNwledge of clinical trial processes, regulations, and ICH-GCP guidelines. + Strong organizational and ... clinical development. We are currently seeking a Clinical Research Associate II Specialist to join...protocol compliance, data integrity, and patient safety throughout the trial process. + Collaborating with investigators and site staff… more
    ICON Clinical Research (09/14/24)
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  • Oncology Clinical Research Associate

    IQVIA (Clarksville, TN)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines *… more
    IQVIA (09/04/24)
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  • Client Executive, Clinical and Regulatory…

    Astrix Technology (Nashville, TN)
    …space. + Working knowledge of Clinical & Regulatory systems such as Clinical Trial Management System (CTMS), electronic Trial Master Files (eTMF), ... for the sale and growth of Astrix Technology Group's Clinical and Regulatory Consulting services to a portfolio of...representative of those that must be met by an associate to successfully perform the essential functions of this… more
    Astrix Technology (07/16/24)
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  • Associate Director, Programming

    Takeda Pharmaceuticals (Nashville, TN)
    …**How you will** **contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the Programming Center of Excellence) ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Programming in Cambridge, MA, where you will...Standard code, AI and ML applications). + Collaborate with Clinical Trial Transparency Teams to implement data… more
    Takeda Pharmaceuticals (09/14/24)
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