• Merck & Co. (Boston, MA)
    …manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are ... Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for...phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical… more
    HireLifeScience (10/25/25)
    - Save Job - Related Jobs - Block Source
  • Jobleads-US (Bridgewater, MA)
    Sr. Manager/ Associate Director , Global Recruitment Marketing Updated: August 12, 2025 Location: Bridgewater, NJ, United States Job ID: 10794-OTHLOC-Ce9wYfwB ... external partners to deliver high-impact campaigns. Ensure alignment with corporate communications and compliance standards across all global recruitment marketing… more
    Appcast IO CPC (10/29/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director

    Wolters Kluwer (Boston, MA)
    **About the Role:** Together with the Director of Communications for */dxg, the Communications Business Partner serves as the strategic communications advisor for ... a deep understanding of */dxg's goals, priorities, and stakeholders. + Support Director of Communications in co-creating an annual communication plan that support… more
    Wolters Kluwer (10/15/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Regulatory…

    Rhythm Pharmaceuticals (Boston, MA)
    …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible ... cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs . Responsibilities and Duties...multiple audiences This role is based out of our corporate office in Boston, Massachusetts. Rhythm operates in a… more
    Rhythm Pharmaceuticals (09/17/25)
    - Save Job - Related Jobs - Block Source
  • Global Regulatory Affairs Device Lead…

    Sanofi Group (Framingham, MA)
    **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team...regulatory strategies for their products in order to meet corporate and business objectives. + Leads the Device GRT,… more
    Sanofi Group (10/23/25)
    - Save Job - Related Jobs - Block Source
  • Associate Director , Global Health…

    Takeda Pharmaceuticals (Boston, MA)
    …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global Emerging Markets… more
    Takeda Pharmaceuticals (09/30/25)
    - Save Job - Related Jobs - Block Source
  • Associate Medical Director /Medical…

    AbbVie (Boston, MA)
    …deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. + ... opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent… more
    AbbVie (11/04/25)
    - Save Job - Related Jobs - Block Source
  • Senior Director , Clinical Research,…

    Merck (Boston, MA)
    …manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate personnel are ... **Job Description** The Senior Director (Sr. Principal Scientist) has primary responsibility for...phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical… more
    Merck (10/25/25)
    - Save Job - Related Jobs - Block Source
  • Assoc Director , Clinical and Safety…

    Takeda Pharmaceuticals (Boston, MA)
    …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring ... requirements, auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role… more
    Takeda Pharmaceuticals (10/31/25)
    - Save Job - Related Jobs - Block Source