• Associate Director, Bioinformatics

    BeOne Medicines (San Carlos, CA)
    **General Description:** We are seeking an experienced and visionary Associate Director of Bioinformatics to join our Translational Discovery, Research, and Medicine ... team in San Carlos, California. This individual will play a key role in enhancing our bioinformatics infrastructure and capabilities in the United States, providing strategic and technical expertise and leadership to support clinical biomarker analysis and… more
    BeOne Medicines (06/19/25)
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  • Associate Director, Biostatistics

    BeOne Medicines (Emeryville, CA)
    …Skills:** Knowledge of SAS and/or R is strongly desirable **Education Required:** + PhD in Statistics or related field with 4+ years of experience in clinical ... drug development is preferred. Or, Masters with 6+ years' experience. + Knowledge of SAS and/or R is strongly desirable. **Other Qualifications:** Experiences with clinical trials and knowledge of regulatory guidance are required. Oncology experience is… more
    BeOne Medicines (08/27/25)
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  • Quantitative Systems Researcher, Associate

    BlackRock (San Francisco, CA)
    …We remain focused on increasing the impactful moments that arise when we work together in person - aligned with our commitment to performance and innovation. As a new ... **About this role** BlackRock is one of the world's preeminent asset management firms and a premier provider of global investment management, risk management and advisory services to institutional, intermediary, and individual investors around the world.… more
    BlackRock (08/22/25)
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  • Associate Director, Regulatory Affairs…

    Gilead Sciences, Inc. (Foster City, CA)
    …and skills we seek for this role. **Preferred Education & Experience** + PharmD/ PhD with 2+ years' relevant experience. + MA/MS/MBA with 8+ years' relevant ... experience. + BA/BS with 10+ years' relevant experience. + 4+ years' experience in prescription drug labeling. + Significant regulatory experience in the biopharma industry is strongly preferred. + Significant experience working with a broad array of… more
    Gilead Sciences, Inc. (08/22/25)
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  • Associate Director, Clinical Data Science…

    Gilead Sciences, Inc. (Foster City, CA)
    …Ten Years' Experience** **OR** **Masters' Degree and Eight Years' Experience** **OR** ** PhD and Two Years' Experience** **Preferred Qualifications:** + 10 years of ... relevant experience with a BS degree in life sciences or related field with significant experience advising business functions in the biopharma industry on quality and compliance requirements, evolving regulations, risk minimization and mitigation, and vendor… more
    Gilead Sciences, Inc. (08/21/25)
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  • Associate Director, Scientific Publications…

    Gilead Sciences, Inc. (Foster City, CA)
    …Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to ... enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications… more
    Gilead Sciences, Inc. (08/13/25)
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  • Associate Director, Digital Marketing IT…

    Gilead Sciences, Inc. (Foster City, CA)
    …Years' Experience** **OR** **Masters' Degree and Eight Years' Experience** **OR** ** PhD and Two Years' Experience** **Preferred Qualifications:** + Bachelor's Degree ... in Science/ Business / Computer Science / Information Technology + 8 years of overall technology experience with at least 5 years supporting commercial business functions as an IT Commercial Business Partner required + Strong understanding of Commercial Pharma… more
    Gilead Sciences, Inc. (08/12/25)
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  • Associate Director, Regulatory Affairs

    United Therapeutics (Sacramento, CA)
    …area of study or 7+ years of biologic or pharma regulatory experience with a PhD in life sciences, quality, regulatory 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 the ESG portal + Proven track record in successfully navigating regulatory submissions + Proven ability to lead and influence data-driven… more
    United Therapeutics (08/10/25)
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  • Associate Director, Global TA Regulatory…

    Gilead Sciences, Inc. (Foster City, CA)
    …and skills we seek for this role. **U.S. Education & Experience** + PharmD/ PhD with 2+ years' relevant experience. + MA/MS/MBA with 8+ years' relevant experience. ... + BA/BS with 10+ years' relevant experience. + Significant regulatory, quality, compliance or related experience in the biopharma industry. + Proven track record in effectively setting and directing the regulatory or related strategy to successful conclusion… more
    Gilead Sciences, Inc. (08/02/25)
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  • Post Doctoral Associate Chemical Biology

    Lilly (Pasadena, CA)
    …+ Ph.D. in scientific fields of Chemical Engineering, Chemistry, Biochemistry, Biology, or related fields. + Experience with LC-MS and/or MS/MS instrumentation ... At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who… more
    Lilly (07/19/25)
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