• Associate Director , Global…

    BeOne Medicines (San Mateo, CA)
    …proposals together with the regional strategic feasibility teams. Close partnership with global program & study management team for design and delivery of the ... analyses, predictive models, and feasibility risk assessments to inform governance and program /study planning. + Plays a key role in driving the implementation of… more
    BeOne Medicines (09/29/25)
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  • Associate Director , Neuroscience,…

    Bristol Myers Squibb (San Diego, CA)
    …late stage portfolio for regulatory, translational development and life cycle management . Translational Development drives strategy across core therapeutic areas at ... are not limited to, the following:** + Designs and implements program -specific late development biomarker/translational plans, responsible for aiding in creation of… more
    Bristol Myers Squibb (09/28/25)
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  • Associate Director , Global R&D…

    BeOne Medicines (Emeryville, CA)
    **General Description:** This position will be responsible for the management of clinical outsourcing needs in support of BeOne's current and planned clinical trials ... position will also be responsible for clinical study budget estimation and budget management during the study life cycle, engaging the business, and maximizing the… more
    BeOne Medicines (08/27/25)
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  • Global Benefits Associate Director

    WTW (San Francisco, CA)
    …solutions that meet the needs of both local and headquarter management in the design, establishment, financing, operation, oversight and monitoring of ... communication liaison with our clients, create client deliverables, contribute to client management and new business activities, and participate in the creation of… more
    WTW (09/27/25)
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  • Associate Director , Safety…

    BeOne Medicines (San Mateo, CA)
    …continuously, explore the opportunities of doing things differently and smartly **Team Management :** + Manage a team of data scientists and data analysts or ... improvement + Promote data-driven decision-making at the study and program level through hands-on support and stakeholder engagement. **Education/Experience… more
    BeOne Medicines (09/20/25)
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  • Associate Director Quality Assurance

    Takeda Pharmaceuticals (Los Angeles, CA)
    …and ongoing maintenance of prevention-based Quality Systems. These systems include exception management , CAPA, Change Control, and Quality on the Shop Floor, all of ... or biological sciences) + 8+ years of relevant experience, including 3+ years in a management role with direct reports + Deep knowledge of FDA, EMA, CFDA, and PDA… more
    Takeda Pharmaceuticals (08/23/25)
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  • Regulatory Affairs Associate

    GRAIL (Menlo Park, CA)
    …10 years of experience in regulatory, development, clinical affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries. ... and provide direction to regulatory staff and, when required, participate in senior management meetings as a delegate. The role fosters a work culture aligned with… more
    GRAIL (08/16/25)
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  • Associate Director - Business Unit…

    The Clorox Company (Oakland, CA)
    …across core/base business and brands, innovation, category leadership, revenue growth management and other key business growth drivers. . Manages, mines, synthesizes ... in our Clorox community. Learn more about our I&D program & initiatives** here (https://www.thecloroxcompany.com/company/idea/) **.** **[U.S.]Additional Information:** At… more
    The Clorox Company (08/26/25)
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  • Associate Director , Global Security…

    BeOne Medicines (San Carlos, CA)
    …meetings and events, develops and manages the company's event protection program , monitors global threats, and supports the department with real-time intelligence, ... and technical strengths that generate confidence in BeOne's Global Security program internally and externally.** **Essential Functions of the Job:** **Lead security… more
    BeOne Medicines (08/08/25)
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  • Associate Director , Regulatory…

    United Therapeutics (Sacramento, CA)
    …and execution of regulatory submissions for our whole organ tissue engineering program . Are you looking to fundamentally change medicine and transplant science while ... affairs or a related area of study + 8+ years of project or people management experience + Must have written an IND and submitted it in ECTD format through… more
    United Therapeutics (09/27/25)
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