Associate Director, Biostatistics
Tasks
- Author statistical analysis plan
- Conduct internal protocol reviews
- Design clinical trials
- Develop and mentor team members
- Develop protocols
- Draft regulatory submissions
- Interpret trial results
- Manage multiple studies
- Plan statistical analyses
- Prepare clinical study reports
- Present trial results
- Respond to health authority requests
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis planning | Biostatistics | Clinical Trial Design | Clinical study reports | Clinical trial | Data Manipulation | Project Management | Protocol development | Python | R | Regulatory Affairs | Regulatory Submissions | SAS | Statistical Analysis | Statistical Analysis Planning | Trial design
Education
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