• Associate Director , Internal…

    Vera Therapeutics (Brisbane, CA)
    Title: Associate Director , Internal Communications Location: Brisbane, Ca About Us: Vera Therapeutics (Nasdaq: VERA), is a late clinical-stage biotechnology ... reach, including specific communications to different ET organizations (R&D, Commercial, Regulatory , G&A) and different levels (LT, people managers). * Establish… more
    Vera Therapeutics (07/04/25)
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  • Scientific Associate Director - PKDM…

    Amgen (South San Francisco, CA)
    …Join us and transform the lives of patients while transforming your career. **Scientific Associate Director - PKDM (Small Molecule ADME)** **What you will do** ... PK/PD or PBPK + Experience in supporting preclinical components of regulatory documentations. + Excellent interpersonal, technical, and communication skills to lead… more
    Amgen (06/29/25)
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  • Associate Director , Market Access,…

    BeOne Medicines (San Mateo, CA)
    **General Description:** The Associate Director of Market Access Business Strategy is responsible for supporting the development and execution of strategies ... into actionable strategies. + Ability to evaluate the impact of regulatory , legislative, or contracting changes on business performance. + Strong presentation… more
    BeOne Medicines (06/11/25)
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  • Associate Director , Interventional…

    AbbVie (Irvine, CA)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Interventional Glaucoma - Surgical Marketing, is ... from concept review to final approval, via close collaboration with legal, compliance, regulatory and medical. + Represent the US commercial strategy as a member of… more
    AbbVie (06/05/25)
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  • Associate Medical Director

    Evolent (Sacramento, CA)
    …mission. Stay for the culture. **What You'll Be Doing:** Evolent is seeking an ** Associate Medical Director - Cardiovascular Medicine** to play a critical role ... and expedited appeals,** ensuring compliance with UM policies and regulatory requirements. + Collaborate with cross-functional teams, including **clinical reviewers,… more
    Evolent (06/03/25)
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  • Associate Director , Search…

    AbbVie (San Francisco, CA)
    …to ensure an in-depth understanding of the science behind each of these opportunities. The Associate Director , Search & Evaluation will be a key member of the ... one aspect of Drug Development (eg, pre-clinical research, clinical development, Regulatory Affairs, Chemistry Manufacturing and Controls (CMC)). + Experience with… more
    AbbVie (05/28/25)
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  • Associate Director Quality Assurance

    Takeda Pharmaceuticals (Los Angeles, CA)
    …The role is essential in ensuring that all quality-related activities meet regulatory standards and uphold Takeda's commitment to excellence. The incumbent will work ... Quality Systems procedures across departments, driving consistent compliance + Ensure regulatory conformance across multiple operational areas + Identify and resolve… more
    Takeda Pharmaceuticals (08/23/25)
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  • Associate Director , Product…

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …of possible** with us. As a strategic partner reporting to the Sr Director of Global Integrated Supply Chain (ISC), you'll connect platform teams with manufacturing ... **Skills** + Advanced knowledge in operational excellence, quality systems, regulatory compliance, and financial management + Proficiency with ERP systems… more
    BD (Becton, Dickinson and Company) (08/02/25)
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  • Associate Director , Clinical Data…

    Gilead Sciences, Inc. (Foster City, CA)
    …and CAPA management team within Gilead R&D Quality on internal audits, regulatory agency inspections, risk assessment, deviations and CAPA activities + Liaison and ... including authoring and reviewing SOPs, facilitating internal audits, supporting regulatory inspections, developing and managing CAPAs and deviations, and training… more
    Gilead Sciences, Inc. (08/21/25)
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  • Associate Director , Neuroscience,…

    Bristol Myers Squibb (San Diego, CA)
    …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
    Bristol Myers Squibb (07/24/25)
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