Associate Director, Biostatistics
Tasks
- Author regulatory submission documents
- Communicate results to clinical and regulatory partners
- Create analysis plans
- Design clinical trials
- Develop development strategy input
- Develop trial protocols
- Drive interpretation and key messages with clinicians
- Ensure hypotheses and data support analyses
- Ensure statistical deliverable quality
- Interpret clinical trial results
- Keep up with applied statistical methodology
- Lead biostatistics project teams
- Provide statistical consultation for ad hoc analyses
- Select study populations and endpoints
- Size trials cost effectively
- Translate scientific questions into statistical terms
Perks/Benefits
- Employee assistance program
- Flexible work environment
- Healthcare benefits
- Hybrid work option
- Paid time off
- Retirement savings plan
- Wellness programs
Skills/Tech-stack
Analysis Plan | Biostatistics | Case Report Forms | Clinical Trial Design | Clinical study reports | Clinical trial | Clinical trials | Data Manipulation | Data Presentation | Graphing | HTA | Hypothesis Testing | Protocol development | Python | R | Regulatory Submissions | SAS | Simulation | Statistical Analysis | Statistical Analysis Plan | Statistical methodology | Tables Listings and Figures | Trial design
Education
Roles
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