• Associate Director

    Rhythm Pharmaceuticals (Boston, MA)
    …commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties ... tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs...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 , Biostatistics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …study report (FSR), including authoring statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study ... products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a...key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Associate Director

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    The Associate Director of Regulatory ...+ Build professional network with key stakeholders outside of Global Regulatory Affairs to identify ... Description** + Oversee the capture, review, and dissemination of global regulatory news, public commenting opportunities, new...technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years'… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Associate Director

    Lilly (Boston, MA)
    …year. Verve is headquartered in Boston, Massachusetts. **The Position** The purpose of the Associate Director , Regulatory Strategy role is to support the ... development and implementation of innovative global regulatory strategies for preclinical and early...submissions, and taking part in meetings. + Represent the regulatory affairs team on cross-functional project teams… more
    Lilly (10/28/25)
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  • Associate Director , Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial functions + Coordinate interdepartmental ... is true to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and… more
    Takeda Pharmaceuticals (09/04/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Marlborough, MA)
    …Master Files (TMFs) ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures accountable ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with … more
    Sumitomo Pharma (11/05/25)
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