Trial Principal, Statistician, Roivant Health
Roivant Sciences, Inc., 1 Pennsylvania Plaza, 54th floor, New York, NY 10119, United States
USD 130K-220K Senior-level Full Time
Tasks
- Analyze clinical trial datasets for efficacy signals and safety patterns
- Apply Bayesian analysis
- Assess competitor trial data
- Build statistical models from scratch
- Conduct subgroup and sensitivity analyses
- Develop shared analytical infrastructure across platforms
- Evaluate endpoint choices and statistical analysis plans
- Integrate literature registries claims and proprietary datasets
- Monitor safety signals in real time
- Perform mixed effects longitudinal analysis
- Run analytical sprints
- Select and integrate data sources including claims labs and genomics
- Synthesize clinical evidence and uncertainty
Perks/Benefits
Skills/Tech-stack
Bayesian statistics | Clinical Trial Data | Clinical trial | Data integration | Evidence synthesis | Genomics | Longitudinal analysis | Machine Learning | Mixed-effects | Mixed-effects models | Safety Signal Monitoring | Sensitivity Analysis | Signal monitoring | Statistical modeling | Statistics | Subgroup Analysis | Trial data
Education
N/A
Roles
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