Principal Biostatistician Consultant- Hybrid (NJ/PA/DE)
Tasks
- Conduct DAR meetings before database lock
- Conduct comment resolution meetings
- Coordinate statistical and programming support
- Create sample size calculations
- Design clinical study protocols
- Draft and review statistical analysis plan
- Lead statistical methodology
- Manage contractors and CROs
- Manage statistical aspects of drug development
- Mentor entry-level team members
- Perform endpoint analysis
- Prepare regulatory submission statistics
- Present and interpret statistical results
- Review TLF outputs for consistency
Perks/Benefits
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical study | Clinical trial | R | Regulatory Submission | SAS | Sample Size | Sample Size Calculation | Statistical Analysis | Statistical Analysis Plan | Study design | TLF
Education
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