- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director Global Regulatory Lead, GRAD Oncology. You will provide ... global regulatory strategies in collaboration with their regional counterparts. + As the Associate Director , you will be responsible for complex or highly… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as Associate Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. ... lead to drive a MIDD path within each project. + Leads strategic, scientific , and operational aspects of multiple drug development projects with a high level… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 TAU ... within our Global Regulatory Affairs organization, based remotely. + Partners with the Global...in the USA or more jurisdictions. + Understanding of scientific principles and regulatory standards/requirements relevant to global drug… more
- Sanofi Group (Cambridge, MA)
- **Job title** : GRA Device Lead ( Associate Director ) **Location:** Cambridge. MA **,** Morristown, NJ **About the Job** Are you ready to shape the future of ... Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research and Development. The… more
- Takeda Pharmaceuticals (Lexington, MA)
- …application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US Medical** ... execution of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be responsible for the ... the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global Device Sub team...and executes a labeling implementation plan to incorporate new scientific , safety and clinical data, as well as Health… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being...Engages with partner global functions (eg Clinical Science, Med Affairs , Regulatory Affairs , Biostats) to ensure alignment… more
- 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 ... the drug's value proposition will be recognized among the external ( scientific / payer influencing/HTA expert) stakeholder community and hence market access and… more
- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** ... deadlines. **Education / Experience Requirements** + Bachelor's degree required; advanced scientific degree preferred (Masters, PhD, PharmD, BSN, etc.) with at least… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director , TLL, Renal Rare Disease, is a field-based, customer facing, non-sales position on Otsuka's Rare Renal team focused on enhancing and ... The TLL will work closely with cross-functional leaders from Marketing, Medical Affairs , Sales, Key Accounts, Market Access, Patient Access and the Renal Leadership… more