Offer summary
Qualifications:
MS required; Ph.D. preferred in Biostatistics or Statistics., 6+ years experience in drug development., Experience with neuromuscular diseases preferred., Familiarity with regulatory submissions strongly preferred., Hands-on experience with SAS and R programming..
Key responsabilities:
- Lead development of statistical study protocols and analysis plans.
- Optimize trial designs for registrations through strategic input.
- Collaborate with cross-functional teams for timely deliverables.
- Oversee CRO activities and manage contractors effectively.
- Communicate complex statistical concepts to diverse audiences.