Senior Principal Statistician, Biometrics
Parsippany, New Jersey, United States
USD 191K-225K Senior-level Full Time
Tasks
- Advise on statistical rigor
- Analyze RWE studies
- Analyze and interpret clinical trial data
- Analyze subgroups and sensitivity results
- Assess asset value and lifecycle management opportunities
- Author statistical analysis plans
- Conduct RWE studies
- Conduct independent analyses of key endpoints
- Contribute to regulatory submissions
- Contribute to study design
- Create Clinical Study Reports
- Create integrated evidence generation strategies
- Design RWE studies
- Evaluate readiness for regulatory submission
- Perform gap analyses for missing data
- Provide statistical input to clinical development plans
- Report RWE results
- Review clinical trial data for efficacy and safety
- Support HTA and lifecycle planning
- Support RWE regulatory submissions
- Support due diligence reports
- Validate asset potential
Perks/Benefits
- Flexible benefits
- Learning and development opportunities
- Paid parental leave
- Reimbursement for tuition
- Wellness benefits
Skills/Tech-stack
Biostatistics | Causal Inference | Clinical trials | Data Analysis | External Control | External control arms | Health technology | Health technology assessment | Observational data | Observational data analysis | R | Real-World Evidence | Regulatory Submissions | SAS | Synthetic control | Synthetic control arms | Target trial emulation | Technology assessment | Trial Emulation
Education
Regions
Countries
States
Cities
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