• Device Regulatory Lead

    Sanofi Group (Cambridge, MA)
    **Job title: Device Regulatory Lead ( Associate Director)** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... thought was possible. Ready to get started? **Main responsibilities** + Serve as Device Regulatory Lead on assigned project teams (early phase, late stage… more
    Sanofi Group (06/06/24)
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  • Associate Director, US Advertising…

    Sanofi Group (Cambridge, MA)
    …the job** The Associate Director, US Advertising and Promotion serves as the regulatory lead on Review Committees (RCs). As the RC Regulatory Affairs ... **Job title: Associate Director, US Advertising and Promotion, Global Regulatory Affairs** + Location: Cambridge, MA or Bridgewater, NJ **About… more
    Sanofi Group (06/19/24)
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  • Associate Clinical Lead Director…

    IQVIA (Boston, MA)
    …to subject/patient recruitment and on time high quality data collection. The Clinical Lead provides leadership of the clinical team, in support of the project ... for Request for Proposals (RFPs). + Participate in bid defense preparations. Lead the Clinical delivery strategy at bid defense presentations in partnership with… more
    IQVIA (06/07/24)
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  • Field Clinical Lead , CoreValve - East…

    Medtronic (Boston, MA)
    …Medical Education, Global Field Training, Clinical Research, Research and Development, Regulatory and Legal. **A DAY IN THE LIFE - POSITION RESPONSIBILITIES:** ... updated best practices within region + Develops therapy and device operational knowledge and applies this knowledge to processes...as the District Expert and function as the District Lead for simulation + Collaborates with the Global Field… more
    Medtronic (05/22/24)
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  • Program Associate Director

    Zimmer Biomet (Braintree, MA)
    …respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to enable the ... key functional areas - Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio as owned by… more
    Zimmer Biomet (05/30/24)
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  • Site Quality Leader

    J&J Family of Companies (Bridgewater, MA)
    …and product release for Medical Devices. In addition, the Site Quality Lead of Raynham/Bridgewater will identify and facilitate the implementation of key ... related to compliance, technology investments, regulation, and resource management/optimization. The associate partners with Site and Business Unit leaders to drive… more
    J&J Family of Companies (06/14/24)
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  • Senior Manager, Systems Engineering - Combination…

    Amgen (Cambridge, MA)
    …colleagues in identification of user needs from market insights. The SMSE will lead a team responsible for the creation and management of system requirements, ... across the interactions, dependencies, and interfaces of subsystems. The SMSE will lead a team responsible for the integration of the system through clinical… more
    Amgen (03/29/24)
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  • Sr Clincial Specialist Coronary Renal Denervation…

    Medtronic (Boston, MA)
    …is assigned to the business unit. + Develop and maintain therapeutic and device operation knowledge; apply this knowledge to the development of well-written, clear, ... analyze literature search results + Address deficiencies and or answer questions from regulatory agencies as needed + Create and manage project schedule for each… more
    Medtronic (04/16/24)
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