• Genmab (Plainsboro, NJ)
    …essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director, Global Regulatory Affairs , Regulatory Strategy to be a part of our ... Global Regulatory Affairs organization.In this role, you will...you will work in close collaboration with the Global Regulatory Lead (s) on a compound in late-stage… more
    HireLifeScience (01/25/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …difference? The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks related to ... The ideal candidate will collaborate with cross-functional teams of Regulatory Affairs Therapeutic Area (TA) Managers, Global...Rico Registrations Labeling Tools: Serve as a subject matter expert in all labeling tools (SPL, TVT, Veeva Vault,… more
    HireLifeScience (01/25/25)
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  • Genmab (Plainsboro, NJ)
    …information) for the Genmab portfolio of products. This role will be within Global Regulatory Affairs (GRA) and will report to the Sr Director, Labeling, Policy ... and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading… more
    HireLifeScience (11/15/24)
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  • Genmab (Plainsboro, NJ)
    Affairs Solid Tumors Strategy will report to the Senior Director, US Medical Affairs Solid Tumors Strategy Lead . S/he will provide medical affairs ... US healthcare market through collaboration with US Commercialization, Global Medical Affairs , Clinical Development, Regulatory , and other cross functional… more
    HireLifeScience (12/11/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    affairs , market access and policy/advocacy (MAPA), Centers of Excellence (COEs), regulatory affairs , and other relevant NNI departments to ensure alignment ... to experiment with us? The Position The Integrated TA Lead is instrumental in shaping and executing NNI's strategic...updates to leadership Product Evolution: Oversee product strategy and regulatory activities related to new clinical data or label… more
    HireLifeScience (02/01/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    affairs , market access and policy/advocacy (MAPA), Centers of Excellence (COEs), regulatory affairs , other relevant NNI departments, and external stakeholders ... experiment with us? The Position The HCP - Strategy Lead (MASH) lead will be a pivotal...life cycle activities Health Systems strategy: Collaborates with medical affairs and market access teams to inform a health… more
    HireLifeScience (12/14/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Access and Public Affairs (MAPA), Portfolio Strategy, Commercial Excellence, Regulatory Affairs , and other relevant NNI departments to ensure alignment ... embark on shaping our future. The Position The Rare Bleeding Therapeutic Area Lead is instrumental in shaping and executing NNI's strategic direction and initiatives… more
    HireLifeScience (12/19/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …access, commercial insights and analytics, sales, medical/CMR, legal, compliance, and regulatory . Other internal relationships include Public Affairs , Government ... Managers, and Market Access), Brand Marketing, Training, Market Access & Public Affairs , Trade, Legal, Compliance, Finance, HEOR, and Market Research. The position… more
    HireLifeScience (01/11/25)
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  • Lead Expert Regulatory

    dsm-firmenich (Princeton, NJ)
    ** Lead Expert Regulatory Affairs Pet Food** **Location: Plainsboro, NJ** **Hybrid** Are you a junior Regulatory Affairs professional ready to ... in this niche space where you can learn and grow. We are hiring a Lead Expert Regulatory Affairs Pet Food to support our Taste Texture and Health (TTH)… more
    dsm-firmenich (11/27/24)
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  • Director, Global Regulatory Affairs

    Merck (North Wales, PA)
    **Job Description** The Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory ... Global Process Lead actively engages with leadership across the Global Regulatory Affairs and Clinical Safety organization and collaborates with internal and… more
    Merck (01/10/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Trenton, NJ)
    …seeking a dynamic, highly motivated, and experienced individual for the position of **Director Regulatory Affairs ** . The Director is part of the Global ... Regulatory Affairs (GRA) team based in the...I-IV Research & Development Activities + As a Regional Regulatory Lead , manage regional (United States and/or… more
    Sumitomo Pharma (11/28/24)
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  • Vice President, Head of Medical Affairs

    Sumitomo Pharma (Trenton, NJ)
    …of scientific and medical information for key stakeholders. The Vice President will lead the global medical affairs functions for investigational and marketed ... medical affairs activities for investigational and marketed products. + Lead development of systems and processes to ensure harmonized and integrated medical… more
    Sumitomo Pharma (11/16/24)
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  • Director, Medical Affairs Strategy…

    Sumitomo Pharma (Trenton, NJ)
    …and responses to unsolicited requests for medical/scientific information. + Serves as Medical Affairs Lead on select therapeutics topics, and provides input into ... management peri-, pre-, and post-launch activities related to Medical Affairs function. This individual will lead program...Product Development Monthly Meetings. + Serve as Subject Matter Expert within Medical Affairs Team provide medical… more
    Sumitomo Pharma (11/27/24)
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  • Senior Director, Medical Affairs Strategy…

    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. The job ... external facing HCP and Payer interactions. The Sr. Director of Medical Affairs develops and maintains professional relationships with key physicians and other… more
    Sumitomo Pharma (11/21/24)
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  • Senior Manager, Medical Affairs Technology…

    Sumitomo Pharma (Trenton, NJ)
    …and experienced individual for the position of **Senior Manager, Medical Affairs Technology and Digital Innovation** . **Job Duties and Responsibilities** + ... Supports the development, implementation, execution, and oversight of Medical Information/Medical Affairs digital services and innovative digital projects as well as… more
    Sumitomo Pharma (12/14/24)
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  • Senior Director, Regulatory Medical Writing

    J&J Family of Companies (Spring House, PA)
    …Clinical Operations, Medical Affairs Operations, Global Medical Safety, Global Regulatory Affairs and Operations, Human Resources, Talent Acquisition, IT, ... & Johnson Innovative Medicine is recruiting for a Senior Director, Regulatory Medical Writing to be located in Springhouse, Pennsylvania, Allschwil, Switzerland,… more
    J&J Family of Companies (02/04/25)
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  • Regulatory and Accreditation Specialist

    Penn Medicine (Bala Cynwyd, PA)
    …and TJC accreditation standards suggested.Working under the leadership of the Director of Regulatory and Patient Affairs and close association with the Penn ... meetings, staff-focused formal presentations/discussions, and daily/team instruction to reinforce regulatory documentation requirements. + Demonstrate as an expert more
    Penn Medicine (01/18/25)
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  • Therapeutic Area Lead - Rare Bleeding

    Novo Nordisk (Plainsboro, NJ)
    …Access and Public Affairs (MAPA), Portfolio Strategy, Commercial Excellence, Regulatory Affairs , and other relevant NNI departments to ensure alignment ... our future. The Position The Rare Bleeding Therapeutic Area Lead is instrumental in shaping and executing NNI's strategic...outcomes + Product Evolution + Oversee product strategy and regulatory activities related to new clinical data or label… more
    Novo Nordisk (12/19/24)
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  • Global Labeling Lead (Sr. Scientist)…

    Merck (North Wales, PA)
    …on labeling to teams. + As the regulatory labeling liaison on global Regulatory Affairs subteams, your input will be essential to our operations. + You ... of labeling experience or relevant pharmaceutical industry experience (eg, Medical Affairs , Regulatory Affairs , Clinical, Pharmacovigilance). Current… more
    Merck (01/15/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Plymouth Meeting, PA)
    …cross-functional colleagues in preclinical science, data science, clinical operations, regulatory affairs , chemistry, manufacturing and control (CMC), project ... in the US** The Director, Translational Medicine and Early Development (TMED) Lead will be responsible for contributing and/or devising the early clinical… more
    Organon & Co. (01/28/25)
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