• Associate Director, Global Product Quality - GMP…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …(CAPA), Deviations, and Change Control** , ensuring compliance with global regulatory requirements and internal standards. The successful candidate will lead ... alignment with corporate quality objectives + Cross-functional Leadership:Collaborate with Regulatory Affairs, Technical Operations, Manufacturing, and Supply Chain to… more
    Otsuka America Pharmaceutical Inc. (12/10/25)
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  • Director I, Aesthetics Clinical Development

    AbbVie (Irvine, CA)
    …author, edit and review key section of research protocols, reports and regulatory submissions. Responsibilities: + Based on strong medical and scientific experience, ... knowledge of compliance and regulatory requirements, Allergan Aesthetics customers, markets, business operations and emerging issues , manage the design and… more
    AbbVie (12/09/25)
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  • Senior 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 (12/09/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …overall implementation of assigned research protocols, ensuring efficiency and regulatory compliance. Key responsibilities will include recruiting and screening ... Case Report Forms, as well as reporting serious adverse events and managing drug accountability, supplies, and equipment. The CV Med Clinical Research Team (CCRT) is… more
    Stanford University (11/11/25)
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  • Senior Scientific Director, Clinical Development…

    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 (11/07/25)
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  • Senior Hydrogeologist Job Details | Black & Veatch…

    Black & Veatch (San Marcos, CA)
    …as wellfield development, aging wellfield infrastructure, rehabilitation, operations, regulatory compliance, aquifer storage and recovery systems, injection wells, ... intrusion, brackish groundwater development and treatment, brine management, and evolving regulatory frameworks. This role is ideal for someone who thrives in… more
    Black & Veatch (11/06/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and ... assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will… more
    Stanford University (11/06/25)
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  • Energy Analyst (Economics) - Immediate Hire

    The Brattle Group (San Francisco, CA)
    …consulting firm. We provide expert analysis and testimony in legal disputes, regulatory proceedings, and business strategy. Our teams apply economic, financial, and ... decisions in areas such as corporate finance, energy, competition, and regulatory economics. **WHAT IS ECONOMIC CONSULTING** Economic consulting involves using… more
    The Brattle Group (10/30/25)
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  • Manager, PVRM

    Sumitomo Pharma (Sacramento, CA)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
    Sumitomo Pharma (10/30/25)
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  • Clinical Research Coordinator Associate

    Stanford University (Stanford, CA)
    …to the coordination of clinical research studies. Studies may include drug / device trials, longitudinal natural history studies, and other PI-initiated projects ... enroll and follow patients on trial and assist with regulatory and financial requirements of the trials. We are...as the primary contact with research participants, sponsors, and regulatory agencies. + Assist with the screening, recruiting, and… more
    Stanford University (10/25/25)
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