• Clinical Trials Regulatory

    Stanford University (Stanford, CA)
    Clinical Trials Regulatory and Quality Specialist **School of Medicine, Stanford, California, United States** **New** Research Post Date 1 day ago ... Fixed Term 12 months Stanford University is seeking aClinical Trials Regulatory and Quality Specialist... clinical trials operations, knowledge of clinical trials regulatory requirements, or… more
    Stanford University (04/17/25)
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  • SCCC Clinical Research Coordinators…

    University of Miami (Miami, FL)
    clinical trials for its catchment area. We provide administrative, regulatory , clinical , laboratory, quality , and training services to investigators ... clinical research and regulatory professional positions. CRS is Sylvester's centralized clinical trial office, supporting cutting edge Phase 1-3 oncology… more
    University of Miami (03/04/25)
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  • Regulatory , Clinical ,…

    Alaka'ina Foundation Family of Companies (Frederick, MD)
    Regulatory , Clinical , and Technical Clinical Trial support Location MD - Frederick Job Code 10393 # of openings 1 Apply Now ... need for top talent to provide Regulatory , Clinical , and Technical Clinical Trial ...and Social Science Support - Positions may include: Biostatistician; Clinical Data Manager/ Regulatory Writer; Quality more
    Alaka'ina Foundation Family of Companies (03/26/25)
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  • Clinical Research Nurse Manager

    Actalent (Atlanta, GA)
    …and maintain awareness of all relevant clinical research projects. + Ensure clinical and regulatory quality and integrity of research conducted. + ... research operations. This role will manage and oversee the quality and validity of clinical research data...but not required. + Experience in cardiovascular, cardiology, management, clinical trials , and data management. + Maintain… more
    Actalent (04/16/25)
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  • Manager, Clinical Supply Chain

    BeiGene (San Mateo, CA)
    … Study Teams (CST) and provide a high service level to internal stakeholders (eg Clinical Operations, Regulatory , Quality , CMC). + Work with Clinical ... + Create supply and inventory plans and develop production schedules for clinical trial materials. + Monitor schedule adherence of production schedules… more
    BeiGene (04/05/25)
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  • Sr. Specialist, Clinical Supply Project…

    Merck (Rahway, NJ)
    …for clinical supplies. + Interacts with key partner organizations such as clinical development, regulatory , quality and other supply chain areas to ... supply chain across our Company's Research Laboratories portfolio of clinical trials . GCS is accountable for the...spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related… more
    Merck (04/10/25)
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  • Associate Director, Clinical Supply Project…

    Merck (Rahway, NJ)
    …with key partner organizations(as a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas ... clinical supply chain across our Company's Research Laboratories portfolio of clinical trials . GCS is accountable for the planning, sourcing, labeling,… more
    Merck (04/10/25)
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  • Senior Clinical Research Director, Pain

    Medtronic (Minneapolis, MN)
    …with sales & marketing management as well as other functions including, regulatory , clinical , quality , reimbursement, research and development, ... responsible for designing and driving the execution of pre-market and post-market clinical trials globally, including driving outcomes and results, and… more
    Medtronic (04/05/25)
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  • Manager, Global Clinical Supply Chain

    Gilead Sciences, Inc. (Foster City, CA)
    …to develop clinical supply strategies and plan with the focus on delivering compliant, quality IMP to clinical trials globally on time in full. + Ensures ... . Works collaboratively within the department and with cross functional colleagues (eg, Regulatory , Clinical Operations, Quality , PDM sub-teams, GSC, etc.)… more
    Gilead Sciences, Inc. (04/11/25)
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  • Exec. Director/Vice President, Clinical

    Surrozen (South San Francisco, CA)
    …close collaboration with multidisciplinary teams including preclinical development, biostatistics, clinical operations, quality , regulatory affairs and ... with study investigators . Assist in the preparation of clinical sections of key regulatory documents, including...(eg FDA, EMA, etc.) * Thorough working knowledge of clinical trial design, methodology, and statistical concepts… more
    Surrozen (04/04/25)
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