Principal Statistician, Biostatistics
US - Home-Based, United States
R
USD 132K-198K Senior-level Full Time
Tasks
- Attend regulatory agency meetings
- Collaborate on clinical reports
- Create statistical programs
- Design clinical trials
- Develop statistical contributions to regulatory filings
- Develop statistical strategy
- Develop study protocols
- Oversee biostatistics and programming vendors
- Perform statistical analysis
- Prepare data displays
- Respond to regulatory agency questions
- Review and validate CRO deliverables
- Review clinical data capture systems
- Simulate clinical trial operating characteristics
- Validate statistical analyses
- Verify data accuracy
- Write Statistical Analysis Plans
Perks/Benefits
Skills/Tech-stack
Adaptive clinical trial design | Bayesian statistics | CDISC ADaM | CDISC SDTM | Clinical Trial Design | Clinical trial | Data Validation | Hypothesis Testing | ICH Guidelines | Nonparametric Models | Parametric Models | Programming validation | R | SAS | Sample Size | Sample Size Calculation | Statistical inference | Trial design
Education
Roles
Biostatistician | Principal | Principal Statistician | Statistician
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