Associate Director, Biostatistics
Tasks
- Author statistical documents
- Defend protocols and analysis plans
- Design clinical trials
- Develop and advise team members
- Develop protocols
- Develop statistical analysis plans
- Ensure compliance with SOPs
- Lead statistical community of practice
- Manage multiple studies
- Plan analysis and interpretation
- Present trial results
- Provide statistical support to regulatory requests
- Review clinical study reports
- Support performance reviews
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis planning | Biostatistics | Clinical Trial Methodology | Clinical trial | Clinical trial protocol | Data Manipulation | Data Visualization | Project Management | Python | R | Regulatory science | SAS | SOP compliance | Simulation | Statistical Analysis | Statistical Analysis Planning | Statistical programming | Trial methodology
Education
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