Global real-world evidence leader with over 20 years of experience shaping evidence strategies across multiple therapeutic areas, health care systems, and diverse data assets.
- Directs natural history studies to inform clinical trial design, endpoint selection, and regulatory submissions.
- Integrates evidence generation and scientific communications with regulatory requirements, professional guidelines, patient preferences, safety considerations, and payer value propositions to optimize portfolio life-cycle management.
- Supports pipeline development by evaluating epidemiologic evidence, competitive dynamics, and the data landscape to inform product acquisition decisions.
- Spearheads practical application of novel study designs to accelerate approvals and market access while reducing costs.
Content Area Specialties
- Design and analysis of observational studies to inform clinical trial decision-making
- application of novel study and analysis methods to improve efficiency of clinical trials of therapeutics for approval and access
Methods Specialties
- Causal inference
- external control
- meta-analysis