• Cipla (Fall River, MA)
    …committee, commercial, portfolio, R&D technical staff, supply chain management, medical affairs , regulatory affairs , quality assurance, procurement etc. ... only - is not for those applying for a global assignment and/or for employees working outside of Cipla's...In collaboration with Cipla commercial, supply chain management and regulatory affairs , responsible for launch planning, launch… more
    HireLifeScience (10/22/25)
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  • Merck & Co. (Boston, MA)
    …and executing integrated development plans that align clinical, medical affairs , commercial, manufacturing, regulatory , analytical, and epidemiological ... DescriptionOur Clinical Research and Pharmacovigilance team pushes the boundaries of global healthcare through research and innovation. Through clinical trials and… more
    HireLifeScience (10/30/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Cambridge, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion ... prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you… more
    Takeda Pharmaceuticals (10/29/25)
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  • Associate Director , Global

    Sanofi Group (Cambridge, MA)
    **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are ... thought was possible. Ready to get started?​ **Main Responsibilities:** + Represents Global Regulatory Affairs (US RA AdPromo) as a member of… more
    Sanofi Group (10/24/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion ... GRA A&P SME for assigned products and projects. + Regulatory advisor as the "R" in the core Medical,...and implementation + Product or project business lead for global CMRP at Takeda + CMRP Meeting Chair- pausing… more
    Takeda Pharmaceuticals (10/28/25)
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  • Associate Director - Analytics,…

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** **Job Title:** Associate Director - Analytics, Global Regulatory Affairs **Role Purpose:** Strategic and operational ... oversight of custom analytics deliveries from Global Regulatory Affairs involving Business Intelligence solutions and related semantic layer dependencies.… more
    Takeda Pharmaceuticals (10/14/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Boston, MA)
    …my knowledge. **Job Description** **Objective / Purpose:** + Defines, develops and leads global strategies to maximize global regulatory success towards ... + Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of … more
    Takeda Pharmaceuticals (08/12/25)
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  • Director , Global Regulatory

    Takeda Pharmaceuticals (Boston, MA)
    …and approves - as needed - technical protocols, reports, etc. to ensure alignment with global regulatory requirements and standards. + When in a GRA CMC Product ... tactical regulatory guidance to product teams in line with global regulatory strategies. Accountable for development and / or commercial products approvals… more
    Takeda Pharmaceuticals (10/30/25)
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  • Associate Director , Regulatory

    Rhythm Pharmaceuticals (Boston, MA)
    …commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties ... to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you...execution of regulatory filings, maintaining compliance with global regulatory standards and commitments. You will… more
    Rhythm Pharmaceuticals (09/17/25)
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  • Associate Director , Regulatory

    Sumitomo Pharma (Boston, MA)
    Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will primarily ... function as a regional regulatory leader (RRL) and/or Global ...Ideally with a minimum of 4 years focused in regulatory affairs + Oncology product development experience… more
    Sumitomo Pharma (10/11/25)
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