Associate Director, Pharmacoepidemiology Analytics
Current- Lead evidence/business insights generation across all phases, including identifying evidence gaps, designing studies, defining endpoints, executing research, and publishing results, to support late-stage or post-market.
- Lead statistical analyses of real-world data (RWD) using claims and electronic medical records (EHR) databases, registries and clinical trial data.
- Develop and execute epidemiological studies in support of regulatory filings such as Postmarket Requirements and Commitments (PMRs/PMCs), Post-Authorization Safety Studies (PASS), Post-Authorization Efficacy Studies.