• Senior Principal Scientist, Translational…

    Merck (Boston, MA)
    …of Phase I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, ... insight into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human… more
    Merck (09/03/25)
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  • Principal/Sr Principal Scientist, Hematology…

    Bristol Myers Squibb (Cambridge, MA)
    …for assigned programs. Key responsibilities of this role are to act as a lead scientist to deliver and implement biomarker strategies for clinical programs, ... plans working with laboratory and disease scientists and BMS members from clinical , medical, commercial, regulatory and diagnostics as well as engage external… more
    Bristol Myers Squibb (08/08/25)
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  • Associate Director, Global Regulatory Affairs…

    Sanofi Group (Cambridge, MA)
    …, medical, safety, and regulatory colleagues to provide labeling input relevant to clinical study protocols, especially in early and late development phases. + ... of global labeling strategy for assigned products, including those in clinical development, life cycle management (LCM), and the marketed portfolio. This… more
    Sanofi Group (06/27/25)
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  • Associate Director - Principal Medical Writer

    Sanofi Group (Cambridge, MA)
    …Demonstrated expertise in clinical development processes + Strong understanding of clinical study methodology and basic statistics + Knowledge of regulatory ... started? **Main responsibilities:** _Document Development_ + Create high-quality regulatory-compliant clinical documents supporting product life cycle + Ensure timely… more
    Sanofi Group (07/31/25)
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  • Regulatory Strategist

    Sanofi Group (Cambridge, MA)
    …HA preferred. + Experience on multidisciplinary matrixed project teams (eg clinical study team) preferred. + Project leadership experience preferred. ... Global Regulatory Team (GRT), and strategic partner to the Global Regulatory Lead (GRL), the Regulatory Strategist (RS) leverages their regulatory expertise to… more
    Sanofi Group (09/06/25)
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  • Winter-Spring 2026 Co-op-Intern- CMC Biologics…

    Sanofi Group (Framingham, MA)
    …biologic drug products and manufacturing processes. Our team works from lead candidate identification and selection through clinical development and ... and process development. The Co-Op/Intern will be exposed to laboratory-based studies working on different facets of drug product development, including formulation… more
    Sanofi Group (07/13/25)
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  • Technical Service Research Supervisor

    Charles River Laboratories (Cambridge, MA)
    …& Development Labs (CRADL) in vivo technical service and research group . Provides supervision and training for employees. Maintains performance and service ... responsibilities include: + Supervises the daily activities of technical services and study team comprising of research associate/ study technicians and study more
    Charles River Laboratories (08/08/25)
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  • Physician Executive for the Cardiovascular Service…

    Tufts Medicine (Boston, MA)
    …patient outcomes through an integrated cardiovascular research pipeline. There are currently 58 clinical studies (48 active and 10 in start-up). Within the CVCRI ... governance, academic and research structure. Tufts Medicine is comprised of the following clinical entities: + Tufts Medicine Professional Group (TMPG) + Tufts… more
    Tufts Medicine (07/14/25)
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  • Associate Director, Precision Disease Genetics

    Merck (Cambridge, MA)
    **Job Description** The Complex Disease Genetics group within the Data, AI and Genome Sciences (DAGS) Department at our Company is seeking an accomplished Associate ... and precision medicine. As a member of the Precision Disease Genetics group , you will leverage advanced statistical genetics methodologies to analyze large-scale… more
    Merck (08/26/25)
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  • Associate Director, Vendor Management (Commercial…

    Takeda Pharmaceuticals (Lexington, MA)
    …Product Sourcing) may also contribute actively to cross functional teams as required. + Lead Global Clinical Supply Chain group initiatives including the ... to facilitate the procurement and management of comparator drugs within Global Clinical Supply Chain (GCSC). Under the direction of the Director of Centralized… more
    Takeda Pharmaceuticals (08/13/25)
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