- Takeda Pharmaceuticals (Cambridge, MA)
- …plans or study designs that may have a significant impact on timelines or product labeling. Synopsis / Protocol Development , Study Execution, & Study ... you to shine? Join us as an Executive Medical Director in our GI & Inflammation Therapeutic Area Unit...MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being… more
- Sanofi Group (Cambridge, MA)
- …with regulatory requirements and Sanofi's product positioning. The Associate Director contributes to early development activities by providing regulatory ... **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy...race is on to speed up drug discovery and development to find answers for patients and their families.… more
- Takeda Pharmaceuticals (Boston, MA)
- …or study designs that may have a significant impact on timelines or product labeling. Plans clinical development strategies in context of medical/clinical ... you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At...our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being… more
- Catalent Pharma Solutions (Chelsea, MA)
- …unparalleled service to pharma, biotech, and consumer health customers, supporting product development , launch, and full life-cycle supply. With time-tested ... Director of Quality Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …anticipate trends that impact both the regulatory and access environments to strengthen product development plan(s) and adopt regulatory strategies in a timely ... MSc, PhD, PharmD, MD). BA acceptable with significant Industry experience. + Sr Director 12+ years of pharmaceutical industry experience inclusive of 10 years… more
- Sumitomo Pharma (Boston, MA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... of early- to late-stage assets, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, ... : Reporting to the Vice President, Global Medical Affairs, the Executive Director , CNS Strategy, Global Medical Affairs is a leadership position responsible for… more
- Takeda Pharmaceuticals (Boston, MA)
- …products and labeling guidance and trends at portfolio level to drive the development of essential, innovative, industry-leading product labeling to patients and ... in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for the … more
- Sanofi Group (Cambridge, MA)
- …to the Global organization as needed. + Contributes US RA AdPromo input to the development of optimal FDA product labeling on original and supplemental New Drug ... **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location**...race is on to speed up drug discovery and development to find answers for patients and their families.… more
- Takeda Pharmaceuticals (Lexington, MA)
- …c) Reference Standard Management; d) GMP Quality Systems + Contribute to product development from Research to Commercialization by collaborating with multiple ... within the Pharmaceutical Science organization to improve analytical, process and product knowledge. Including the support of transfer of development assets… more