Company Summary
This position with one of the largest, most cutting-edge pharma companies in the world where you would have the opportunity to work in a small team specifically focused with the intent to accelerate innovation for people with Rare Blood Disorders.
Responsibilities
- Create regulatory strategies to ensure efficiency and effectiveness of clinical development for rare disease indications
- Prepare, lead and develop briefing materials for US FDA meetings
- Assist in the development of submission documentation to ensure successfully submissions (IND/NDA/BLA)
- Supervise, coach mentor junior staff
