Sabrina is a seasoned project management and regulatory affairs professional with over 20 years of experience guiding pharmaceutical and biotech companies through the complexities of drug development. She has successfully led programs across a wide range of therapeutic areas, managing projects through every stage—from early-phase planning to final product approval. Sabrina excels at steering cross-functional teams with precision and agility, ensuring efficient project execution and delivering high-quality outcomes, while leveraging her broad regulatory insight to navigate an intricate industry landscape. Sabrina obtained a Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professional Society (RAPS) and received a BS in Pharmaceutical Science from Massachusetts College of Pharmacy.