Offer summary
Qualifications:
PhD/MS in Stats or related field with 5+/7+ years industry experience, Regulatory submission and statistical software proficiency required.
Key responsabilities:
- Provide statistical support for drug development programs
- Interact with project teams, write protocols and analysis plans
- Monitor project activities, contribute to regulatory documents
- Review study reports, supervise programmers, interpret results
- Collaborate with various teams, participate in development activities