• Associate, PhD (Economics Focus)

    The Brattle Group (Boston, MA)
    …Brattle is large enough to be sought after to answer complex economic, regulatory , and financial questions for clients around the world. We are also small ... enough to provide our Associates with a variety of experiences and individualized development from our experts. Associates are central members of each project team… more
    The Brattle Group (10/21/25)
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  • Research & Development Director

    ICP Group (Andover, MA)
    …Pacific region. ICP Group is seeking an experienced R&D Director to lead our research and development efforts at our Andover, MA facility. This individual will ... Collaborate with senior management to align R&D objectives with business strategy. Product Development & Innovation: + Direct the research and formulation of new… more
    ICP Group (11/19/25)
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  • Vice President, Regulatory Affairs…

    Sumitomo Pharma (Boston, MA)
    …a diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For ... HTA submissions. The individual will be responsible for leading development of all non-clinical and clinical regulatory ...the Marketing Brand Teams, Legal, Medical Affairs and Clinical Research in the development of advertising and… more
    Sumitomo Pharma (12/23/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Cambridge, MA)
    …scientific background, PhD ., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years. + Scientific & ... risk mitigation planning. + Cultivate inclusive, high-impact collaboration with Precision Medicine, Research teams, Global and Regional Regulatory Leads, Global … more
    Bristol Myers Squibb (11/24/25)
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  • Senior Director, Clinical Research

    Merck (Boston, MA)
    development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May Be ... study reports, or publication + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
    Merck (01/10/26)
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  • Clinical Director (Principal Scientist), Clinical…

    Merck (Boston, MA)
    …post-licensure). The Director will manage the entire cycle of clinical development , including study design, initiation, monitoring, analysis, regulatory ... study reports, or publication; and + Participation in internal and joint internal/external research project teams relevant to the development of new compounds,… more
    Merck (01/09/26)
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  • Vice President, Translational Research

    Rhythm Pharmaceuticals (Boston, MA)
    …of non-clinical studies supporting IND, early clinical development , and regulatory submissions. + Represent non-clinical research in regulatory ... role requires extensive cross-functional engagement with senior leaders in clinical development , regulatory affairs, data sciences, and commercial functions to… more
    Rhythm Pharmaceuticals (12/03/25)
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  • Snr Research Consultant

    Oracle (Boston, MA)
    …from home** Oracle Life Sciences is seeking a qualified health outcomes researcher with a PhD to join our Health Outcomes Research team in the Real World ... the job and/or completed higher education; preferred PharmD with health outcomes research , PhD in pharmaceutical sciences, epidemiology, health outcomes, or… more
    Oracle (01/07/26)
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  • Post Doctoral Research Fellow

    Tufts Medicine (Boston, MA)
    …securing research funding by contributing to grant writing and research proposal development . 8. Collaborates with healthcare professionals and institutions ... new discoveries. The successful candidate will have: - MD, PhD or both required - Excellent writing and communications...to collect clinical data and samples for research purposes. 9. Contributes to the development more
    Tufts Medicine (01/11/26)
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  • Clinical Research Director, Immunology…

    Sanofi Group (Cambridge, MA)
    …GCP, ICH guidelines and other regulations + Review documents supporting clinical development such as Investigator's brochure, regulatory documents for IND / ... CTA, clinical sections of integrated development plans, and submission dossiers for regulatory ...research + Represent Sanofi at scientific conferences and regulatory meetings **About You** **Experience / Skills:** + MD… more
    Sanofi Group (12/09/25)
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