About me
I’m a pharmacoepidemiologist with 13 years of experience in the biotechnology industry. My background includes five years in drug safety operations, which continues to strongly inform my current work. I bring hands-on experience with real-world evidence to support pharmacovigilance and safety commitments, including descriptive and comparative safety analyses and risk management planning. I enjoy partnering closely with Patient Safety, RWE product leads, and cross-functional teams to advance study design and generate evidence that ultimately benefits patients.
