Associate Director, Biostatistics
Tasks
- Apply statistical clinical trials methodology
- Author statistical analysis documents
- Collaborate with cross-functional teams
- Design clinical trials
- Develop performance metrics
- Develop protocols
- Interpret study results
- Manage multiple studies
- Plan statistical analysis
- Prepare clinical study reports
- Present data and analysis results
- Provide leadership to team members
- Respond to health authority requests
- Review protocols and analysis plans
- Support regulatory submissions
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis planning | Biostatistics | Clinical Development | Clinical trials | Data Manipulation | Graphing | Leadership | Project Management | Protocol development | Python | R | Regulatory strategy | SAS | SOP compliance | Simulation | Statistical Analysis | Statistical Analysis Planning | Statistical Reporting | Trial design | Written communication
Education
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