Global Regulatory Affairs, Drugs & Biologics (2 years)
The fellow will receive mentorship from the Global Regulatory Affairs Development team and will collaborate with cross-functional project teams, as well as GlobalHealth Authorities. Additionally, the fellow will acquire a better understanding of the global drug development process through participation in various activities in the United States, the European Union, Japan, and emerging markets. Fellows will be providing regulatory support in these potential therapeutic areas: Neuroscience, Rare Diseases, Oncology, and Plasma-Derived Therapies.
Location: Cambridge, MA
Number of positions available: 3
Current Fellows:
Additional Resources:
Learn More About Takeda's Plasma-Derived Therapies Business Unit