Upvote
Downvote
Associate Director - Global Regulatory Lead
Share Job
- Suggest Revision
Full-time
- Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development.
- We are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple innovative modalities and therapeutic areas.
- Our East Coast Global Development Hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.
- Perform regulatory review of all clinical and nonclinical documents for submissions, e.g., clinical protocols and study reports, preclinical reports, investigator brochures, application summary documents, etc.
- Effectively managing timelines while working in a fast-paced and dynamic environment across both time zones and cultures
Active Job
Updated TodaySimilar Job
Relevance
Active