Advance patient outcomes and business objectives through real-world evidence data analysis
Requirements
- Experience using RWD in regulatory filings, post-marketing studies, or pharmacovigilance
- Deep knowledge of claims-based data sources (e.g., Optum, HealthVerity) and their use in oncology research
Responsibilities
- Support development and critical appraisal of study protocols using RWD (claims, EHRs, registries)
- Partner with Biostatistics and Programming to build statistical analysis plans using both descriptive and complex designs
- Lead or support generation of code lists and RWD algorithms through literature reviews and collaboration
- Conduct and support data analysis and quality control using healthcare databases
- Review data thoroughly to ensure completeness, reliability, and integrity
Other
- Master’s or PhD in Epidemiology, Biostatistics, Statistics, or related field
- 4+ years of experience with real-world data in pharma, CRO, or academia
- 4+ years of oncology research experience highly preferred
