Associate Director I/II, Real World Data Statistics
Tasks
- Apply causal inference methods
- Build propensity score models
- Create regulatory grade statistical analysis plans
- Design implement validate survival analysis
- Develop longitudinal modeling
- Ensure EMA registry guidance alignment
- Ensure FDA RWE framework alignment
- Ensure reproducibility and audit readiness
- Handle missing data and confounding
- Lead cross functional collaboration for regulatory submissions
- Manage data linkage and cohort construction
- Mentor Real World Data statisticians
- Oversee registry evidence strategy
- Produce tables figures listings and briefings
- Support external investigators and regulatory consultants
Perks/Benefits
- N/A
Skills/Tech-stack
Audit Readiness | Causal Inference | Confounding | Data linkage | Longitudinal Modeling | Missing data | Propensity Score Matching | Propensity score | Python | R | Real-World Evidence | Reproducibility | SAS | SQL | Score Matching | Survival analysis
Education
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