• Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee ... Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC . **How you will contribute:** + Plan, execute and manage regulatory… more
    Takeda Pharmaceuticals (07/08/25)
    - Related Jobs
  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US Medical** ... cross-functional clinical programs within Medical Affairs, Clinical Research, Regulatory, CMC or other drug development related function. Clinical Science experience… more
    Takeda Pharmaceuticals (08/02/25)
    - Related Jobs
  • Associate Director , Analytical…

    Takeda Pharmaceuticals (Lexington, MA)
    …to bring Better Health and a Brighter Future to people worldwide. As an Associate Director in Analytical Development, you will lead efforts to develop advanced ... Process Development, Regulatory, Quality, and external partners (CROs/CDMOs) to achieve CMC objectives and meet program timelines. + Represent Analytical Development… more
    Takeda Pharmaceuticals (07/02/25)
    - Related Jobs
  • Associate Director , Search…

    AbbVie (Cambridge, MA)
    …to ensure an in-depth understanding of the science behind each of these opportunities. The Associate Director , Search & Evaluation will be a key member of the ... research, clinical development, Regulatory Affairs, Chemistry Manufacturing and Controls ( CMC )). + Experience with conducting due diligence exercises within a… more
    AbbVie (05/28/25)
    - Related Jobs
  • Associate Director , NPI Product…

    AbbVie (Worcester, MA)
    …strategic programs; including Brand Teams, New Product Introductions, Product Transfers, CMC , Global Strategic Sourcing, Due Diligence, Site Selection, and Approvals ... and Continuous Improvement. Provides support and interfaces directly/indirectly with the FDA, EMA, MHRA, ANVISA, MoH, etc. for pre-approval inspections. Qualifications + Bachelor's Degree in relevant Life Science or other technical required. Graduate degree… more
    AbbVie (07/09/25)
    - Related Jobs
  • Sr Compliance RCM & Coding Auditor

    Humana (Boston, MA)
    …mitigate risks. The Senior Clinical Compliance Professional will support the Director of Compliance, by ensuring compliance with governmental requirements for ... pharmacy knowledge a plus + Certified Coder (CPC, CRC, and/or CMC ) + Experience with metrics and reporting **Additional Information** **Work-At-Home Requirements:**… more
    Humana (08/23/25)
    - Related Jobs
  • Senior Research Manager, US Medical

    Takeda Pharmaceuticals (Lexington, MA)
    …US Medical Clinical Research, RPE position is as follows: + Partner with Director , Research Process Excellence, RPE to support process for US Medical Research ... members (including US Medical Therapeutic Area Medical Directors, Scientific Associate Directors, Liaisons, external investigators) to resolve and discover cause… more
    Takeda Pharmaceuticals (08/22/25)
    - Related Jobs
  • Project/Program Manager - HBMA

    Shuvel Digital (Boston, MA)
    …Has supervisory and developmental responsibilities within a functional area. The program director manages one or more projects or programs, may manage an operating ... Desired Relevant Certifications: + Project Management Professional (PMP) + Certified Associate in Project Management (CAPM) + Program Management Professional (PgMP)… more
    Shuvel Digital (07/02/25)
    - Related Jobs