Sr Principal Statistician
US - Home-Based - NC, United States
R
USD 156K-234K Senior-level Full Time
Tasks
- Act as statistical subject matter expert
- Contribute to clinical reports and integrated summaries
- Design clinical trial studies
- Develop and implement study protocols
- Develop statistical strategy
- Interpret statistical results
- Perform statistical analysis and validation
- Prepare data displays
- Respond to statistical questions from regulators
- Review and validate CRO deliverables
- Review data capture systems and validation
- Simulate clinical trial operating characteristics
- Support regulatory agency meetings
- Verify data accuracy and validity
- Write Statistical Analysis Plans
Perks/Benefits
Skills/Tech-stack
Adaptive Design | Bayesian analysis | CDISC | Clinical Trial Design | Clinical trial | Hypothesis Testing | Nonparametric Models | Parametric Models | R | SAS | Sample Size | Sample Size Calculation | Trial design
Education
Roles
Biostatistician | Principal | Principal Statistician | Statistician
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