Senior Principal Statistician, Biometrics
Parsippany, New Jersey, United States
USD 191K-225K Senior-level Full Time
Tasks
- Advise on statistical rigor in due diligence
- Analyze RWE studies
- Analyze clinical trial data
- Author clinical study reports
- Conduct RWE studies
- Conduct independent analyses of endpoints
- Contribute to study design
- Design RWE studies
- Develop integrated evidence generation strategies
- Develop statistical analysis plans
- Evaluate asset readiness for regulatory submission
- Interpret clinical trial data
- Perform gap analyses
- Perform independent analyses of sensitivity results
- Perform independent analyses of subgroups
- Prepare regulatory submissions
- Report RWE studies
- Review clinical trial data for efficacy and safety
- Support regulatory evidence generation
Perks/Benefits
- 401(k) plan match
- Flexible benefits
- Paid Holidays
- Paid parental leave
- Paid time off
- Tuition reimbursement
- Wellness benefits
Skills/Tech-stack
Analysis Plan | Biostatistics | Causal Inference | Claims data | Clinical Data Analysis | Clinical data | Clinical trials | Data Analysis | External Control | External control arms | FDA guidance | Observational data | Observational data analysis | R | Real-World Evidence | Registry data | SAS | Statistical Analysis | Statistical Analysis Plan | Statistics | Synthetic control | Synthetic control arms | Target trial emulation | Trial Emulation
Education
Regions
Countries
States
Cities
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