Lead real-world evidence studies for pharmaceutical clients using complex clinical, molecular, claims, EHR, and registry data. Design observational analyses, derive endpoints, apply survival analysis and causal inference methods, interpret results, and communicate findings to technical and non-technical stakeholders. Develop reusable analytical code and standards while incorporating LLMs and agentic workflows into research processes. Collaborate cross-functionally to improve data quality, products, and RWE methodologies, with a focus on oncology and clinical development.

Lead real-world evidence studies using complex clinical and molecular data, observational study design, survival analysis, causal inference, and machine learning. Collaborate with pharmaceutical partners, derive clinical endpoints, interpret results, develop reusable analytical code, and apply LLM-based tools to accelerate workflows. Communicate findings to technical and non-technical stakeholders through reports, presentations, manuscripts, and conference materials while partnering cross-functionally to improve data quality and analytical practices.