• (Senior) Clinical Research Associate

    IQVIA (Carlsbad, CA)
    …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 (07/14/25)
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  • Clinical Research Associate

    Teleflex (Wayne, PA)
    …**Position Summary** Under the supervision of the Clinical Trial Manager, Clinical Operations, the Clinical Research Associate will assist with study ... Clinical Research Associate **Date:** Sep 23, 2025 **Location:** Wayne, PA, US **Company:** Teleflex **Expected Travel** : More than 50% **Requisition ID**… more
    Teleflex (09/24/25)
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  • Associate Medical Director/Principal…

    ThermoFisher Scientific (Las Vegas, NV)
    …abnormalities, changes in patient medical status, and unblinding requests) during a clinical trial . + Assesses reported adverse events and determines causality ... to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is an office-based position for… more
    ThermoFisher Scientific (08/21/25)
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  • Senior Clinical Research Associate

    Danaher Corporation (Chaska, MN)
    …planning and execution of clinical trials in addition to the management of clinical trial sites to ensure compliance with SOPs, protocols, FDA, ICH, and ... Danaher Business System which makes everything possible. The Senior Clinical Research Associate plays an integral role...applicable regulations. This position reports to the Sr. Manager, Clinical Site Operations and is part of the … more
    Danaher Corporation (09/30/25)
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  • Associate Director, Clinical Program…

    Takeda Pharmaceuticals (Boston, MA)
    …Breach review board meetings. + Lead complex quality investigations impacting the clinical trial delivery systems. + Provide Quality Leadership for Serious ... true to the best of my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring… more
    Takeda Pharmaceuticals (07/16/25)
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  • Clinical Research Associate

    Translational Research in Oncology (Los Angeles, CA)
    … research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing ... If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO… more
    Translational Research in Oncology (08/22/25)
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  • Medical Records Technician- Clinical

    Veterans Affairs, Veterans Health Administration (Grand Junction, CO)
    …Responsible for reviewing the overall quality and completeness of clinical documentation. Applies comprehensive knowledge of medical terminology, anatomy & ... health services and the organizational structure to ensure proper code selection. Reviews clinical documentation and provides education to clinical staff on both… more
    Veterans Affairs, Veterans Health Administration (09/10/25)
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  • Associate Clinical Research…

    Ochsner Health (New Orleans, LA)
    …and/or supports data coordinator, including query resolution. + Conducts daily work and clinical trial activity in accordance with Good Clinical Practice ... job evaluates, initiates, and maintains activities related to the conduct of clinical trials with the assistance and guidance of departmental staff. Communicates… more
    Ochsner Health (09/18/25)
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  • Clinical Research Associate

    Touro University (Hawthorne, NY)
    Overview Responsible for pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen ... management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities + Assist in new IRB… more
    Touro University (07/24/25)
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  • Associate Director- Clinical Trials,…

    Lilly (Indianapolis, IN)
    …▪ Bachelor's degree ideally in a scientific area ▪ Minimum 5 years of clinical trial data experience in drug development in areas intersecting (eg ... remote - a generous relocation package can be included with offer The ** Associate Director- Submission Data Delivery** role leads all aspects of global consistency… more
    Lilly (09/23/25)
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