• Pathologist Liaison

    Roche (Boston, MA)
    …Next Generation Sequencing (NGS), and Companion Diagnostics. + Experience in Medical Affairs within an IVD or pharmaceutical company. + Experience with ... The role of the Pathologist Liaison in Medical Scientific Affairs is to serve as a key scientific expert,...we can deliver life-changing healthcare solutions that make a global impact. Let's build a healthier future, together. Roche… more
    Roche (09/06/25)
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  • Plasma Center Nurse - RN ($3,000 Sign on Bonus)

    BioLife Plasma Services (West Springfield, MA)
    …support plasma center operations. BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role: Every day, the donors you meet will ... The Medical Support Specialist follows guidance provided by BioLife Medical Affairs and provides center level support of environmental, health and safety… more
    BioLife Plasma Services (08/08/25)
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  • Plasma Center Paramedic - EMT-P

    BioLife Plasma Services (West Springfield, MA)
    …support plasma center operations. _BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd._ **About the role:** ** ** Every day, the donors you ... The Medical Support Specialist follows guidance provided by BioLife Medical Affairs and provides center level support of environmental, health and safety… more
    BioLife Plasma Services (08/08/25)
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  • Director, Patient Services and HUB

    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 ... Access Marketing, Brand, Data & Analytics, Legal, Compliance, Medical Affairs , IT, and other cross-functional teams to ensure alignment...protected by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with… more
    Sumitomo Pharma (08/15/25)
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  • Manager, PVRM

    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 ... testing) or any other characteristic protected by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US… more
    Sumitomo Pharma (08/01/25)
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  • Regulatory Strategist

    Sanofi Group (Cambridge, MA)
    pharmaceutical /biotechnology experience, including at least 4 years of relevant Regulatory Affairs experience (regional and global ), in early and late stage, ... teams accelerate progress. As a key member of the Global Regulatory Team (GRT), and strategic partner to the... Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Strategist (RS) leverages… more
    Sanofi Group (09/06/25)
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  • Lead, Environmental Sustainability Collaborations

    Takeda Pharmaceuticals (Lexington, MA)
    …alignment between various stakeholders (eg, Global Manufacturing & Supply Communications, Global Corporate Affairs , Global Finance, Global ... **Job Description** **About the role:** As a leading member of Takeda's Global Environment and Sustainability Team, this role works to develop and implement… more
    Takeda Pharmaceuticals (08/02/25)
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  • Senior Manager of Statistics- CMC

    Takeda Pharmaceuticals (Cambridge, MA)
    …for Takeda clinical and biomarker assay development and validation. + Collaborate with Global Manufacturing, Regulatory Affairs , and Global Quality to ... of Chemicals, Manufacturing, and Controls (CMC) study data throughout Pharmaceutical Sciences. We seek an innovative and inquisitive statistician, excited… more
    Takeda Pharmaceuticals (09/03/25)
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  • Associate Director, Clinical and Safety Quality…

    Takeda Pharmaceuticals (Boston, MA)
    …Minimum of 7 years of increasing responsibility and relevant experience in the global pharmaceutical industry in functions such as Clinical Operations, Data ... 3 years of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU,… more
    Takeda Pharmaceuticals (07/25/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Cambridge, MA)
    …medicine and human target validation plan is essential. We are an innovative global healthcare company with one purpose: to chase the miracles of science to ... (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development… more
    Sanofi Group (07/29/25)
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