• Director, Translational Medicine, Immunology (MD…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    **About Us** Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health ... develops, manufactures and markets innovative products, with a focus on pharmaceutical products to meet unmet medical needs and nutraceutical products for… more
    Otsuka America Pharmaceutical Inc. (07/09/25)
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  • Senior Staff Engineer, Modeling

    Takeda Pharmaceuticals (Boston, MA)
    …& results within global SMPD. + Develop project or significant technical strategy and leverages technical skill(s) as a resource/expert within the department. + ... predictions. + Review, interpret and communicate data cross functionally within pharmaceutical sciences and project teams. + Significant technical responsibility for… more
    Takeda Pharmaceuticals (08/29/25)
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  • Director, Clinical Data Management Medical Coding

    Takeda Pharmaceuticals (Boston, MA)
    …Clinical Data Operations & Standards. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... bold mission. **GOALS:** **Responsible for designing and implementing the medical coding strategy for Takeda clinical trial data, including staffing model and vendor… more
    Takeda Pharmaceuticals (08/30/25)
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  • Manager, Analytics & Data Engineering, Onsite

    AbbVie (Worcester, MA)
    …, governance and analytics. This role will lead and implement a site strategy in compliance with regulatory and AbbVie global expectations, champion key ... to lead site analytics web and data quality initiatives within our pharmaceutical operation reporting into Digital Systems organization. This role is central to… more
    AbbVie (07/12/25)
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  • US Executive Director, Medical Affairs,…

    Merck (Boston, MA)
    …growth opportunities and drive innovation. + In-depth expertise in local regulatory frameworks, ethical standards, and pharmaceutical compliance requirements. + ... responsible for the creation and execution of the overall therapeutic aligned US strategy and Country-Medical Affairs Plans (CMAP). The USMA ED is also responsible… more
    Merck (08/20/25)
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  • Validation Lead(ALM) : QA Life Sciences(Hybrid)

    Cognizant (Boston, MA)
    …**_Qualifications_** 10+ years of experience in Testing & Validation within the pharmaceutical or life sciences domain, with a focus on digital transformation and ... and Computer Software Assurance (CSA) processes Knowledge on ALM Test management tool Regulatory Knowledge: Strong understanding of FDA, EMA, GxP, and 21 CFR Part 11… more
    Cognizant (08/27/25)
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  • Executive Director, Commercial Manufacturing

    Sumitomo Pharma (Boston, MA)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... improvement and operational excellence at CMOs. + Develop and Lead Drug Substance Strategy that includes areas for process improvements which lead to cost savings… more
    Sumitomo Pharma (08/02/25)
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  • Head, Analytical Controls (Sr. Director)

    Takeda Pharmaceuticals (Lexington, MA)
    …of analytical controls and compliance + Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all project-related analytical ... to Commercialization by collaborating with multiple functions within the Pharmaceutical Science organization to improve analytical, process and product knowledge.… more
    Takeda Pharmaceuticals (06/06/25)
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  • Executive Medical Director, Oncology Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …Sciences in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... **:** Responsible for ensuring ongoing review and agreement of the Therapy Area Strategy and associated documents formulated by the OTAU leader prior to their review… more
    Takeda Pharmaceuticals (07/28/25)
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  • Principal Scientific Advisor

    Charles River Laboratories (Wilmington, MA)
    …an experienced professional with expertise in establishing effective scientific and regulatory strategies to advance new medicines through the various stages of ... products. Successful individuals have knowledge of domestic and international regulatory expectations and requirements; and can provide intellectual input in… more
    Charles River Laboratories (08/27/25)
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