• HEVA Business Partner

    Sanofi Group (Cambridge, MA)
    …to identify strategies that will improve the impact of research and build advocates for data + Serve as a subject matter expert to provide input in various ... COAs. + Understands, creates, and applies relevant methods (eg, observational data , post hoc analysis of clinical trials, meta-analysis, indirect comparison, etc..)… more
    Sanofi Group (08/22/25)
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  • Manager, PVRM

    Sumitomo Pharma (Boston, MA)
    …limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties and ... and ensure patient safety. + Assist in signal detection activities including data assembly, signal validation, and signal evaluation. + Perform literature monitoring… more
    Sumitomo Pharma (08/01/25)
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  • Senior Manager, Clinical Project Management

    Sumitomo Pharma (Boston, MA)
    …to ensure proper execution and conduct of the clinical trial; generates quality clinical data . + Serves as primary contact and resource for CRO and vendor personnel ... trials including budget and timelines. + Monitors the status of clinical data collection of assigned clinical trials. + Prepares potential investigator site lists… more
    Sumitomo Pharma (09/03/25)
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  • Director, Regulatory Advertising & Promotion

    Sumitomo Pharma (Boston, MA)
    …for assigned products. This position is responsible for providing strategic, expert guidance on the advertising and promotion of assigned products, balancing ... and approval of promotional materials, eg Marketing and their Agencies, Legal , Compliance, and Medical Affairs. + Provide appropriate oversight of promotional… more
    Sumitomo Pharma (07/08/25)
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  • Head of Contracts & Pricing

    Takeda Pharmaceuticals (Boston, MA)
    …implementing procedures to align cross-functional teams amongaccess, government pricing, legal , marketing and compliance operations + Leading Pricing Governance ... of senior leadership from sales,patient value & access, marketing, finance and legal ) that is responsible forthe pricing and contracting strategy across all US… more
    Takeda Pharmaceuticals (07/12/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Boston, MA)
    …of clinical trials, including monitoring of clinical trial safety and laboratory data . + Generates safety queries, evaluates safety data and contributes/authors ... safety statements as a medical safety subject matter expert (SME) on behalf of PVRM for: Study Protocols,...(PADER, PSUR, PBRER, DSUR, IND/NDA Annual Reports), Company Core Data Sheets (CCDS), Locally approved labels such as, United… more
    Sumitomo Pharma (08/15/25)
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  • Director, Global Library Services

    Takeda Pharmaceuticals (Boston, MA)
    legal and regulatory requirements, including copyright laws and data privacy regulations. **_DIMENSIONS AND ASPECTS:_** **Technical/Functional (Line) Expertise** ... the transformation of Global Library Services into a digital first, data -enabling capability that powers scientific decision-making across R&D + Update end-to-end… more
    Takeda Pharmaceuticals (08/23/25)
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  • Senior Network Consultant

    CompuCom (Boston, MA)
    …solution and level of estimate development support as an enterprise infrastructure and data center technologies subject matter expert + Contribute to the ... a Cisco Certified Network Professional (CCNP) or Cisco Certified Internetwork Expert (CCIE) with experience in Cisco Enterprise Infrastructure (Routing and… more
    CompuCom (08/21/25)
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  • Associate Director, Scientific Communications…

    Takeda Pharmaceuticals (Boston, MA)
    …to the Scientific Communications Group Lead, Hematology. As a subject matter expert on scientific publications best practices and the development of scientific ... oncology assets based on medical strategies, transparency requirements, and data availability for pre-launch/launch readiness. This position requires a strong… more
    Takeda Pharmaceuticals (07/02/25)
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  • Associate Director, Global Regulatory Affairs,…

    Takeda Pharmaceuticals (Boston, MA)
    …is accountable for management of all assigned programs/products as the internal expert on US and international Codes, guidance, and industry standards pertaining to ... Promotion lead you will act as the Subject Matter Expert for assigned products and projects focusing on advertising...and function as the "R" in the core Medical, Legal , and Regulatory review functions within the Commercial Material… more
    Takeda Pharmaceuticals (08/18/25)
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