• Novo Nordisk Inc. (Plainsboro, NJ)
    …Cambridge and Seattle reflect the full R&D continuum, from early research through late - stage clinical development. Here, we are building for the future, creating ... record in senior Leadership roles, such as Director or Senior Director of a drug development function such as Clinical Drug Development (preferred) or… more
    HireLifeScience (09/04/24)
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  • Associate Director of Translational…

    Bristol Myers Squibb (Princeton, NJ)
    …Required** + Recognized expertise in translational biomarkers in neurology space + Experience in late stage drug development and activities required for and ... Associate Director will be part of the late stage TM group. The individual will...responsible for TM and clinical biomarker activities to support drug development programs in neurodegeneration and neuropsychiatric indications. This… more
    Bristol Myers Squibb (08/16/24)
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  • International Medical Director

    Novo Nordisk (Plainsboro, NJ)
    …in Lexington, MA and Plainsboro, NJ. We support programs from early research through late - stage clinical development. We are building for the future, creating a ... ready to make a difference? The Position The Medical Director serves as the subject matter expert for our...team working with MASH and ALD projects covering clinical drug development from preclinical assessment through Phase 1-4. .… more
    Novo Nordisk (09/04/24)
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  • Director , WWMO, Pan Tumor & Patient Focus…

    Bristol Myers Squibb (Princeton, NJ)
    …activities and lead the cross functional matrix providing medical strategic direction across late - stage assets and indications in oncology. Partner with the WW ... and is responsible to deliver the WWMO strategy for patient focus across late - stage assets and indications in oncology. + Collaborates and co-leads medical… more
    Bristol Myers Squibb (09/01/24)
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  • Associate Director , Global Regulatory…

    Takeda Pharmaceuticals (Trenton, NJ)
    …preferably with 4 Yrs. In Global Regulatory Affairs + Experience working on late stage filings is highly preferred + Advanced education or credentialing ... will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 TAU within our Global… more
    Takeda Pharmaceuticals (08/21/24)
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  • Director , Quality

    Catalent Pharma Solutions (Princeton, NJ)
    …with 16 flexible clean rooms, QC labs, and warehouse space to support late - stage and commercial-scale autologous and allogeneic cell therapy production. The ... Director , Quality **Position Summary** Catalent is a global,...pharmaceutical fields including managerial roles + Experience with sterile drug product manufacturing and drug substance manufacturing… more
    Catalent Pharma Solutions (08/13/24)
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  • Director , Global Pricing and Access…

    Bristol Myers Squibb (Princeton, NJ)
    …candidate will be accountable for developing market access strategy for marketed and late stage pipeline immunology assets, particularly in neurosciences but not ... efforts to ensure successful market access execution. The ideal candidate for this Director role has a deep understanding and application of global/large health care… more
    Bristol Myers Squibb (09/08/24)
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  • Associate Director , Regulatory Affairs…

    Taiho Oncology (Princeton, NJ)
    …experience in developing and implementing regulatory submissions strategy for early and late stage of development products with strong emphasis of approval ... Associate Director , Regulatory Affairs Operations Pleasanton, CA, USA *...Inc., (TOI) projects, provides strategic regulatory operational guidance during drug development, approval, post approval, and commercialization, in coordination… more
    Taiho Oncology (08/21/24)
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  • Scientific Associate Director - Toxicology

    Bristol Myers Squibb (Princeton, NJ)
    …studies. + Act as a Nonclinical Safety representative on early- and late - stage project development teams. + Provides scientifically and strategically sound ... Is responsible for the oversight of the nonclinical safety-evaluation programs for selected drug candidates. + Assists in the proper design and timely reporting of… more
    Bristol Myers Squibb (09/08/24)
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  • Translational Medicine Sr. Principal Scientist…

    Bristol Myers Squibb (Princeton, NJ)
    …submissions and regulatory interactions as needed **Skills/Knowledge Required** + Understanding of late stage drug development + Experience in activities ... and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will...TM Sr. Principal Scientist will be part of the late stage TM group. The individual will… more
    Bristol Myers Squibb (08/17/24)
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  • Senior Manager, Medical Affairs Strategy

    Sumitomo Pharma (Trenton, NJ)
    …products in the US, Canada, and Europe, a diverse pipeline of early- to late - stage assets, and in-house advanced technology capabilities, we aim to accelerate ... of the Medical Affairs team reporting to the Executive Director , Medical Affairs Strategy. In this role, individuals are...Canada, and Europe, a diverse pipeline of early- to late - stage assets, and in-house advanced technology capabilities,… more
    Sumitomo Pharma (08/15/24)
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  • Head of US Medical - Endocrine Medical Affairs…

    Ascendis Pharma (Princeton, NJ)
    …compliant execution of all medical programs and functions associated with the late - stage development and medical aspects of commercialization of endocrine assets ... of experience working in pharmaceutical or biotech Medical Affairs or Clinical Drug Development. . Experience with Medical Affairs activities including but not… more
    Ascendis Pharma (06/16/24)
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