• Regulatory Affairs Associate

    Kelly Services (Irvine, CA)
    ** Regulatory Affairs Specialist** The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs ... in order to facilitate compliance with US and international regulatory requirements. The Regulatory Affairs ...with US and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide … more
    Kelly Services (11/13/24)
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  • Director, Global Body Contouring, Global…

    AbbVie (Irvine, CA)
    …Marlow, UK, or remotely. What Your New Manager Wants You To Know The Associate Director / Director, Global Body Contouring, Global Aesthetics Medical Affairs ... Global Body Contouring, GAMA in partnership with key medical functional teams; the Associate Director / Director will assist in the development and implementation of… more
    AbbVie (09/20/24)
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  • Associate Director, Physician Development…

    AbbVie (Irvine, CA)
    …core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs , Regulatory Affairs , and Clinical Development ... statistics, regulatory , etc.) as they relate to ongoing medical affairs projects. May assist as consultant/liaison with other corporations when working under… more
    AbbVie (10/05/24)
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  • Associate Director, Scientific…

    AbbVie (Irvine, CA)
    … and training experience preferred. + Strong knowledge of Pharma medical affairs , regulatory and compliance guidelines. + Strong scientific background and ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director, Scientific Communications and Training - Aesthetics, leads the… more
    AbbVie (10/25/24)
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  • Finance Associate , R&D Oncology

    Pfizer (San Diego County, CA)
    …business development analysis and can monitor business performance. The R&D Finance Associate role collaborates mainly with Oncology Operating lines and Medical ... Affairs teams by preparing financial information (budgeting, forecasting and...disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of… more
    Pfizer (11/15/24)
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  • Associate Medical Director Neuroscience…

    AbbVie (Irvine, CA)
    …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other program documents. + May serve… more
    AbbVie (10/16/24)
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  • Medical Director Clinical Development Eye Care

    AbbVie (Irvine, CA)
    …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. + May oversee… more
    AbbVie (11/14/24)
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  • Senior Manager, Biostatistics

    Edwards Lifesciences (Irvine, CA)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
    Edwards Lifesciences (10/28/24)
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  • Senior Clinical Data Manager

    Edwards Lifesciences (Irvine, CA)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
    Edwards Lifesciences (11/13/24)
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  • Senior Clinical Data Manager

    Edwards Lifesciences (Irvine, CA)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
    Edwards Lifesciences (10/30/24)
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  • Center Medical Director (CMD)

    CSL Plasma (Anaheim, CA)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... training to other center staff on medically related procedures and practices. + Reviews and signed Medical Staff Associates notebooks weekly, including a review of approximately one out of five screening medical evaluations and unsuitable test result… more
    CSL Plasma (10/14/24)
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