• Senior Principal Scientist, Translational…

    Merck (Boston, MA)
    …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
    Merck (08/16/25)
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  • Medical Science Liason

    Astrix Technology (Boston, MA)
    …Collaboration: Work closely with internal teams such as Clinical Development, Regulatory Affairs , and Commercial to provide medical insights that ... decisions. + Compliance and Reporting: Ensure all activities comply with regulatory standards and company policies, and accurately document interactions and insights… more
    Astrix Technology (08/11/25)
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  • Senior Program Manager, Strategic Project…

    Eversource Energy (Westwood, MA)
    …System Planning, Engineering, Siting, Real Estate, Legal, Project Management, Engagement, Regulatory Affairs , Environmental Affairs , and other internal ... System Planning, Engineering, Siting, Real Estate, Engagement and Equity, Regulatory , Procurement, Legal, Scheduling, and later\-stage Project Management\. This role… more
    Eversource Energy (07/30/25)
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  • Program Manager, Strategic Project Development…

    Eversource Energy (Westwood, MA)
    …System Planning, Engineering, Siting, Real Estate, Legal, Project Management, Engagement, Regulatory Affairs , Environmental Affairs , and other internal ... System Planning, Engineering, Siting, Real Estate, Engagement and Equity, Regulatory , Procurement, Legal, Scheduling, and later\-stage Project Management\. This role… more
    Eversource Energy (06/04/25)
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  • Associate Director, Device Clinical Development

    Takeda Pharmaceuticals (Lexington, MA)
    …+ Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial functions + Coordinate interdepartmental ... deliver device clinical outcomes that exceed quality benchmarks and regulatory standards. **Core Responsibilities:** **Device Clinical Strategy & Risk Management:**… more
    Takeda Pharmaceuticals (06/06/25)
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  • Chief Medical Officer (CMO)

    Beth Israel Lahey Health (Winchester, MA)
    …external affiliations to stay informed on emerging trends in healthcare quality, regulatory affairs , organizational behavior, and leadership. + Upholds all ... a member of the executive leadership team responsible for the overall medical affairs related to health care delivery. The CMO fosters collaboration across academic,… more
    Beth Israel Lahey Health (08/24/25)
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  • Principal Scientist, Biointerfaces…

    ConvaTec (Lexington, MA)
    …project work + **Scientific & Technical Labs** to execute testing, as required. + ** Regulatory Affairs ** to collaborate on requirements as well as gain early ... including Applied Research, New Product Development, Marketing, Medical and Clinical Affairs , Market Access, and External Innovation, to develop technologies that… more
    ConvaTec (07/22/25)
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  • Associate Vice President, Companion Diagnostics

    Merck (Boston, MA)
    …immunology, neurology, cardiometabolic and others as needed by the pipeline. + Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx development,… more
    Merck (08/19/25)
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  • Director, Quantitative Clinical Pharmacology Lead

    Takeda Pharmaceuticals (Cambridge, MA)
    …Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... approaches (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in meetings with global or… more
    Takeda Pharmaceuticals (06/27/25)
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  • Manager, PVRM

    Sumitomo Pharma (Boston, MA)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
    Sumitomo Pharma (08/01/25)
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