• Senior Learning Business Partner, Global…

    BeOne Medicines (San Mateo, CA)
    …Bachelor's degree in life sciences with minimum of 7 years of experience in pharmaceutical or biotechnology across clinical trial operations. Minimum 2 years of ... years of experience in in training, process improvement, and/or project management required. + Experience in clinical ...required. + Experience in clinical operations as clinical research associate, clinical study manager more
    BeOne Medicines (11/08/25)
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  • Senior Clinical Research Associate

    BeOne Medicines (Emeryville, CA)
    …with general and study-specific monitoring issues * Provide direct support to the Clinical Study Manager by assisting with monitoring visit report review and ... site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with… more
    BeOne Medicines (09/17/25)
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  • Clinical Data Associate

    University of Southern California (San Diego, CA)
    …issues. + Collaboration: Liaison with the clinical team such as the CRAs, Project Manager , Analytical Developers, Lead Data Managers, clinical sites and ... database lock under the direction of the Lead Data Manager . + Collaborates with the lead Data Manager...related bachelor's degree + 1.5 years of experience in clinical trials at a pharmaceutical , biotechnology, or… more
    University of Southern California (11/19/25)
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  • Manager , R&D Applications

    Sumitomo Pharma (Sacramento, CA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Manager , Clinical Systems R&D IT Business Applications** who will serve as ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in...the primary liaison between R&D Clinical Operations team and IT, responsible for the delivery… more
    Sumitomo Pharma (11/15/25)
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  • Senior Manager , Study Start Up - FSP

    Parexel (Sacramento, CA)
    …CRA, Clinical Trial Manager or similar having worked on global clinical trials. + Experience in project management, CRO experience, change management or ... plan. Where delays occur, they will work with the Project Teams/Oversight Manager to mitigate delays and...activities in the matrix, by working closely with the Clinical Trial Manager and CRO counterparts. +… more
    Parexel (11/27/25)
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  • Manager , Medical Core Content - Neph…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    The Manager , Medical Core Content is a team-level operational role responsible for the development, maintenance, and day-to-day quality assurance of all core ... on the execution and production of scientific assets, ensuring they accurately reflect clinical data, adhere to the core scientific narrative, and are compliant with… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • RWD Engagement Manager

    Norstella (Sacramento, CA)
    RWD Engagement Manager Company: MMIT Location: Remote, United States Date Posted: Nov 10, 2025 Employment Type: Full Time Job ID: R-1558 **Description** Why ... on. **About The Role:** As a Norstella RWD Engagement Manager , you will lead the day to day execution...lead the day to day execution of a client project to help clients achieve their goals. You'll work… more
    Norstella (11/11/25)
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  • Senior Manager , Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …in regulatory affairs or related areas (eg, clinical development, project management, quality assurance, etc.) in pharmaceutical or healthcare related ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed. Works… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Senior Manager , CDM Systems Administrator

    BeOne Medicines (Emeryville, CA)
    …to detail and accuracy + Proven problem-solving skills + Demonstrated knowledge of clinical and pharmaceutical drug development process + Experience of ... Senior Manager , CDM Systems Administrator is responsible for leading...+ Manage user, site and subject administration support to clinical applications utilized by Clinical Data Management… more
    BeOne Medicines (09/30/25)
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  • Pharmacometrics Senior Manager

    Gilead Sciences, Inc. (Foster City, CA)
    …will include all stages of drug development from first-in human through Phase IV clinical trials. You will be responsible for the conduct as well as interpretation ... cross-functional partners.** **Responsibilities:** **Leading quantitative and innovative strategies within clinical pharmacology to impact MIDD during the life cycle… more
    Gilead Sciences, Inc. (10/13/25)
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