• Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    …activities pertaining to global and local labeling compliance and quality within Global Regulatory Affairs . + Partners with internal stakeholders and ... to the best of my knowledge. **Job Description** The Regulatory Affairs -Labeling, Associate Director is...external CRO partners such as Global Regulatory Compliance, Global Labeling,… more
    Takeda Pharmaceuticals (11/27/24)
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  • Director Global Regulatory

    Takeda Pharmaceuticals (Trenton, NJ)
    …understands probabilities of technical success for the solutions. + Effectively represent the Global Regulatory Affairs (GRA) function in senior level ... for providing strategic guidance and oversight for the delivery of global regulatory strategies to support development of biomarkers, diagnostic tests, devices… more
    Takeda Pharmaceuticals (12/06/24)
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  • Director Global Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …diseases and immune disorders. **Summary:** Responsible for leading and developing global regulatory strategy for assigned development projects. Represents ... global strategy. + Responsible for ensuring aligned global regulatory strategy is endorsed by GPT...relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs + Knowledge of IND, NDA/BLA… more
    Daiichi Sankyo Inc. (12/18/24)
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  • Associate Director , Global

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational ... leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position may...experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Associate Director , Regulatory

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Affairs ** . The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function ... registration strategy of a project in collaboration with the Global Regulatory Leader (GRL). He/she is expected...pharmaceutical industry with minimum of 6 years focused in Regulatory Affairs + Include the qualifications preferred… more
    Sumitomo Pharma (11/21/24)
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  • Director , Regulatory Affairs

    Sumitomo Pharma (Trenton, NJ)
    Regulatory Affairs ** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/she will primarily function ... as the Regional Regulatory Leader (RRL) and/or Global ...pharmaceutical industry with minimum of 8 years focused in regulatory affairs . + Master's degree required (preferably… more
    Sumitomo Pharma (11/28/24)
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  • Associate Director , Regulatory

    Taiho Oncology (Princeton, NJ)
    regulatory affairs management, the incumbent independently prepares and directs global regulatory affairs activities and provides regulatory ... Associate Director , Regulatory Affairs Strategy...Performance Objectives: + Independently directs as well as prepares global regulatory affairs strategies and… more
    Taiho Oncology (11/28/24)
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  • Senior Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …. Brings issues with regard to ways or working or resources to the Head of US Regulatory Affairs and/or Global Regulatory Lead for asset to reach ... issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned...resolution. + Participate in global product team meetings to provide US … more
    Daiichi Sankyo Inc. (11/13/24)
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  • Director , Regulatory Affairs

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus ... on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include… more
    Regeneron Pharmaceuticals (12/11/24)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …or More Years in the pharmaceutical industry required. + 8 or More Years in regulatory affairs + Experience in providing regulatory strategic input into the ... preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory more
    Daiichi Sankyo Inc. (12/01/24)
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  • Associate Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... preparation of US regulatory submissions and provide US regulatory support across all global projects; meet aggressive deadlines to ensure that regulatory more
    Daiichi Sankyo Inc. (12/18/24)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …+ 7 or More Years in the pharmaceutical industry + 4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA **Travel** Ability to travel up to ... preparation of all regulatory submissions and provide regulatory support across all global projects, securing the cooperation of others (team members); meet… more
    Daiichi Sankyo Inc. (11/09/24)
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  • Director , Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. **Job Overview** The Director , Medical Affairs Strategy (Hematology/Oncology) will be a key ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...member of the Medical Affairs team reporting to the Executive Director ,… more
    Sumitomo Pharma (11/27/24)
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  • Senior Director , Medical Affairs

    Sumitomo Pharma (Trenton, NJ)
    Director , Medical Strategy (Rare Disease) will be a key member of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and external facing HCP and Payer interactions. The Sr. Director of Medical Affairs develops and maintains… more
    Sumitomo Pharma (11/21/24)
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  • Sr. Medical Director , Medical…

    Taiho Oncology (Princeton, NJ)
    …such as: Clinical Development, Commercial, Evidence and Value Development, Market Access and Regulatory Affairs to ensure, as needed, alignment and inputs + ... Sr. Medical Director , Medical Affairs Princeton, NJ, USA...we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other.… more
    Taiho Oncology (11/27/24)
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  • Director , Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …, Medical Strategy (Prostate Cancer)** will be a key member of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and advance patient advocacy efforts to ensure that Medical Affairs activities align with patient focused programs. **Job Duties… more
    Sumitomo Pharma (12/05/24)
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  • Associate Director , Field Medical…

    Sumitomo Pharma (Trenton, NJ)
    …. **Job Overview** Associate Director , Field Medical and Scientific ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...key insights obtained from the RDs to the Medical Affairs and other internal stakeholders in a timely manner.… more
    Sumitomo Pharma (12/14/24)
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  • Senior Director , HEOR Medical…

    Bausch Health (Bridgewater, NJ)
    …of HEOR resources to program teams, clinical development teams, market access, and medical affairs teams. + Providing a forum for global HEOR alignment and best ... Join a team! We are a global diversified pharmaceutical company enriching lives through our...drive our collective progress and impact. As a Senior Director in Health Economics and Outcomes Research (HEOR), you… more
    Bausch Health (11/21/24)
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  • Executive Director , Managed Access…

    Bristol Myers Squibb (Princeton, NJ)
    …Collaboration : Serve as the primary point of contact for internal (Medical Affairs , Development, Commercial, Regulatory Affairs , Legal, and Compliance) and ... record of successfully developing, centralizing and managing MAPs across a portfolio. + Regulatory / Compliance Knowledge: In-depth knowledge of global and local… more
    Bristol Myers Squibb (12/19/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the ... implementing process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global more
    Takeda Pharmaceuticals (10/24/24)
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