• Medical Director, Clinical Research

    Sumitomo Pharma (Trenton, NJ)
    …with all relevant ethical, regulatory, and legal standards. + May participate in or lead clinical development contributions to due diligence or other business ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...relevant affiliates. + Work in close collaboration with the late -stage development group. + Perform other duties… more
    Sumitomo Pharma (11/15/25)
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  • Director, Commercial Manufacturing Validation

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... With several marketed products and a diverse pipeline of early- to late -stage investigational assets, we aim to accelerate discovery, research, and development more
    Sumitomo Pharma (12/12/25)
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  • Director, Medical Communications - Rare Diseases

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …the Rare Disease Medical BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development , Regulatory, Commercial) to ... reports directly into the Senior Director, Rare Disease Business Unit Lead . **Job Description** **Key Responsibilities:** ** Global Scientific Communication… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Regulatory Strategist

    Sanofi Group (Morristown, NJ)
    …May be requested to lead GRT meetings. + Contributes to the development of the Global Regulatory Project Strategy (GRPS) and ensures alignment with ... the development and update of the core global dossier/collaborates with regional lead where region-specific...experience (regional and global ), in early and late stage, development of multiple modalities; experience… more
    Sanofi Group (12/24/25)
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  • Senior Director, Medical Communications,…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …the Nephrology & Immunology BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development , Regulatory, Commercial) to ... directly into the Executive Director, Nephrology & Immunology Business Unit Lead . **Job Description** **Key Responsibilities:** ** Global Scientific Communication… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Summer Internship: Law & Leadership Program (Law…

    Bristol Myers Squibb (Princeton, NJ)
    …meetings and reviewing and editing quarterly report on Form 10-Q. **Drug Development Law and Global Manufacturing, Supply and Corporate Transactions Law** ... change. The internship is paid but not expected to lead to an offer of full-time employment. **The program...Develop an understanding of laws and regulations governing product development , including early stage research and late -stage… more
    Bristol Myers Squibb (01/02/26)
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  • Senior Director, Medical Communications CNS

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …with the CNS Medical BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development , Regulatory, Commercial) to ensure ... enterprise-level global and/or US communication strategies for a marketed or late -stage development product, preferably in CNS therapeutic areas + Proven… more
    Otsuka America Pharmaceutical Inc. (11/14/25)
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  • Vice President, Regulatory Affairs - Oncology

    Sumitomo Pharma (Trenton, NJ)
    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 ... and Europe, and a diverse pipeline of early- to late -stage assets, we aim to accelerate discovery, research, and...-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For… more
    Sumitomo Pharma (12/23/25)
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  • Director, Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    …designee. + Prepare project and/or status reports as assigned. + Ensures that development strategies meet global regulatory requirements over the lifecycle of ... + Experience in developing and implementing CMC regulatory strategy for early and late stage of development products with strong emphasis of approval through… more
    Taiho Oncology (12/09/25)
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  • Senior Manager, IT Web Services

    Sumitomo Pharma (Trenton, NJ)
    …us on LinkedIn. We are seeking a highly skilled and collaborative **Senior Manager, Web Development ** to lead the design, development , and support of our ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...marketed products and a diverse pipeline of early- to late -stage investigational assets, we aim to accelerate discovery, research,… more
    Sumitomo Pharma (11/13/25)
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