RWE & HEOR Analyst
Eight-plus years leading observational research and real-world evidence analyses across claims and EHR data at a 150-million-patient scale. I lead statistical analysis plans, integrate multi-source claims and EHR data into decision-ready evidence, and serve as a strategic advisor on data feasibility and study design for sponsors and federal stakeholders.
- 8+
- years in RWE and observational research
- 150M+
- patient records analyzed across claims and EHR sources
- 5+
- RWE studies owned end to end
- 3 mo
- to master the Truveta platform and its Prose coding language
Core expertise
- RWE study design and leadership. Statistical analysis plans, multi-quarter project management from requirements gathering through stakeholder briefings, and mentorship of junior analysts.
- Multi-platform claims and EHR analytics. Truveta, MarketScan, CMS claims, PointClickCare, Premier/PHD, Epic, and Cerner data integrated into a single analytic view.
- Decision-ready reporting. Interactive dashboards and visualizations in Power BI and Tableau for technical and senior non-technical stakeholders.
- Truveta platform subject-matter expertise. One of the first on my team to gain access; mastered Truveta Studio and Prose within roughly three months, then trained five-plus colleagues at junior and senior levels.
Experience
- Lead development and execution of statistical analysis plans for large-scale RWE studies, leveraging 150M+ patient records from claims (MarketScan, CMS) and multi-platform EHR sources (Truveta, PointClickCare, Premier/PHD) to answer questions on vaccine effectiveness, healthcare utilization, and patient outcomes.
- Serve as a subject-matter expert on the US healthcare system, claims, and EHR data, advising on data feasibility, study design, and interpretation of findings.
- Design and maintain ETL workflows and data models that integrate, standardize, and validate multi-source claims and EHR data.
- Build interactive dashboards and reporting solutions in Power BI, Tableau, SharePoint, and Excel/Power Query for both technical and non-technical stakeholders.
- Mentor junior analysts on observational research methods and review their analyses for accuracy and consistency.
- Lead research publications and regulatory/data governance activities, including first authorship of a 2024 JAMDA paper and co-authorship of a 2024 Vaccine paper; independently manage IRB protocols, DUAs, and CMS ResDAC access.
- Managed clinical trial data operations for industry-sponsored Pfizer-BioNTech mRNA vaccine trials, supporting regulatory-quality data review.
- Developed CDISC-compliant SDTM datasets and analysis files supporting regulatory submissions.
- Integrated clinical trial data with the Georgia immunization registry (GRITS) to evaluate real-world effectiveness in community populations.
Built Excel-based surveillance dashboards tracking case counts and percent-positivity for department leadership, and supported the Pinellas County epidemiology team on outbreak data analyses, including percent-positive trends and excess-death analyses.
Extracted and cleaned analysis-ready datasets from EHR pulls, applied multivariable regression to control for confounding, and summarized results in Excel-based visualizations for clinical stakeholders.
Methods, platforms & tools
Independently mastered the Truveta platform, including Prose, within roughly three months of gaining early access, and have since trained more than five colleagues.
See the technical / platform detail