Associate Director, Biostatistics
Tasks
- Analyze trial data
- Apply clinical trial methodology
- Author statistical documents
- Conduct performance feedback
- Design clinical trials
- Develop protocols
- Develop statistical analysis plans
- Ensure study standards compliance
- Interpret analysis results
- Lead and advise team members
- Manage multiple clinical studies
- Participate in regulatory interactions
- Plan and prioritize project work
- Prepare clinical study reports
- Present study summaries
- Provide statistical support
- Review statistical documents
- Support regulatory submissions
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical trials | Data Manipulation | Graphing | Project Management | Protocol development | Python | R | Regulatory Affairs | Regulatory Submissions | SAS | Simulation | Statistical Analysis | Statistical Analysis Plan
Education
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