- Remote, United States
- Remote
- 5+ years
Provide end-to-end regulatory support for pharmaceutical development and commercialization programs, including IND/NDA submission management, health authority interactions, and lifecycle maintenance.
Responsibilities
- Lead or support IND and NDA submission management
- Coordinate health authority meeting requests and correspondence
- Prepare and coordinate lifecycle submissions
- Conduct regulatory intelligence searches
- Prepare global regulatory team materials
Requirements
- Bachelor’s degree in a scientific, technical, or related discipline