- Chemours (Boston, MA)
- …for supporting US federal regulatory affairs engagement with the United States Environmental Protection Agency (USEPA), as well as other select federal ... living depend on Chemours chemistry. Chemours is seeking a ** Director of Regulatory Advocacy** to join our...of the political, economic, and social environment in the United States at the federal level, and… more
- Beth Israel Lahey Health (Woburn, MA)
- **Job Type:** Regular **Time Type:** Full time **Work Shift:** Day ( United States of America) **FLSA Status:** Exempt **When you join the growing BILH team, ... medical staff services in support of credentialing, privileging, governance, regulatory readiness, and professional practice evaluation. The Director … more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Director , US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge, MA or Morristown, NJ **About the job** Are you ready to ... and direct reports. + In conjunction with the Sr. Director /Product Support Head, imparts senior regulatory guidance...+ Assures alignment and consistency in Region NA, A&P policy application within and across therapeutic products; takes into… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** Are you ... Your skills could be critical in helping our teams accelerate progress. The Director , Global Regulatory Affairs - Global Labeling Strategy is responsible for… more
- Takeda Pharmaceuticals (Boston, MA)
- …the regulatory function on cross-functional Global Program Teams. The Senior Director also will lead discussions of regulatory strategy with senior ... the mitigation strategies proposed. + The Sr Director / Director will be accountable for all US ...work well within global teams and success leading cross-functional regulatory work products. **More about us :** At… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is responsible for developing ... innovative global regulatory strategies and providing strategic regulatory guidance...Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) Review ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you will… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple ... efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. + Is a leader both in the department and within… more
- Takeda Pharmaceuticals (Boston, MA)
- …the Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, execute ... therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee...where you will oversee the development and execution of regulatory CMC development and registration strategies. You will be… more
- Sumitomo Pharma (Boston, MA)
- …Regulatory Advertising & Promotion** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US . He/she will primarily function as ... company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.)...the position of ** Director , … more