Offer summary
Qualifications:
PhD or MS in Statistics/Biostatistics, 5+ years industry experience, Regulatory submission experience, Strong SAS and/or R skills, Experience with simulations.Key responsabilities:
- Provide statistical support for drug development programs
- Interact with project teams to establish timelines
- Write statistical sections of clinical trial protocols
- Monitor project activities and review study results
- Collaborate on design of eCRFs and regulatory documents