Associate Director I/II, Real World Data Statistics
Tasks
- Apply causal inference and propensity score methods
- Build longitudinal modeling approaches
- Conduct data linkage and cohort construction
- Create statistical analysis plans
- Design regulatory grade survival analysis
- Develop registry evidence strategy
- Ensure compliance with EMA registry guidance
- Ensure compliance with FDA RWE framework
- Implement missing data and confounding methods
- Lead cross functional regulatory collaboration
- Mentor Real World Data statisticians
- Prepare regulatory briefing documents
- Produce tables figures and listings
- Review code and share technical findings
- Validate registry outcomes
Perks/Benefits
- N/A
Skills/Tech-stack
Causal Inference | Cohort construction | Confounding control | Data Analysis | Data linkage | Longitudinal data | Longitudinal data analysis | Missing data | Outcome Validation | Propensity score | Python | R | Real-World Evidence | Regulatory science | SAS | SQL | Survival analysis
Education
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