• Associate Director , GHEOR Patient-Reported…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Work as part of cross-functional teams-including clinical development, medical affairs , regulatory , and biostatistics-to ensure HEOR contributions are ... patient/clinician reported measures across Cell Therapy portfolio. Support the Executive Director in developing and executing health economic & outcomes research… more
    Bristol Myers Squibb (08/30/25)
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  • Associate Director , Statistics - (Hybrid)

    AbbVie (Florham Park, NJ)
    …projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Associate Director works in partnership ... San Francisco, CA; Irvine, CA; Florham Park, NJ The Associate Director , Statistics provides statistical leadership for clinical development and life-cycle management… more
    AbbVie (08/30/25)
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  • Associate Director , Statistics…

    AbbVie (Florham Park, NJ)
    …of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Statistics - Immunology provides statistical leadership for clinical… more
    AbbVie (07/16/25)
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  • Associate Director , Competitive…

    Sumitomo Pharma (Trenton, NJ)
    …relevant cross-functional stakeholders, including in Commercial, Clinical Development, Medical Affairs , Regulatory , Sales leadership and Finance/IR functions. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma… more
    Sumitomo Pharma (08/20/25)
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  • Associate Director , US Cell Therapy Access…

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of US Access Marketing is responsible for developing and ... for Breyanzi. This individual will report to the Executive Director of US access strategy and will work closely...work closely with other US access functions, such as Global Market Access, HEOR, Pricing and Contracting, Trade and… more
    Bristol Myers Squibb (08/30/25)
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  • Director

    Robert Half Technology (Princeton, NJ)
    …data-backed reimbursement strategies. Collaborate cross-functionally with Market Access, Government Affairs , Legal, Regulatory , Finance, and Commercial teams to ... Description A global biopharmaceutical company with a growing US presence is seeking a Director of Pricing Policy and Analytics to lead pricing policy evaluation… more
    Robert Half Technology (08/08/25)
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  • Associate Director , US Biosimilars…

    Teva Pharmaceuticals (Parsippany, NJ)
    …organization, including forecasting, finance, R&D, business development, market access, legal, and regulatory affairs . **How you'll spend your day** + Market ... Associate Director , US Biosimilars Pipeline Planning and Strategy -...be to ensure operational readiness, working closely with R&D, regulatory and IP to identify and prepare for key… more
    Teva Pharmaceuticals (08/30/25)
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  • Regional CPE Director , Tzield…

    Sanofi Group (Jersey City, NJ)
    **Job Title:** Regional CPE Director , Tzield Mid-Atlantic/Northeast **Location:** Remote, US **About the job** **Role Overview:** The Regional Care Path Educator ... (CPE) Director will join the Type 1 Diabetes Commercial organization...and PCP/PED educational outreach efforts. We are an innovative global healthcare company with a focus on immunology that… more
    Sanofi Group (08/20/25)
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  • Sr Director , Trade and Distribution

    Mitsubishi Chemical Group (Jersey City, NJ)
    …pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several first-in-class medicines ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
    Mitsubishi Chemical Group (07/15/25)
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  • Senior Director , MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Oversee the process validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...+ Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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