Laury Roa

Laury Roa is a Product Manager in Global Regulatory Affairs at MSD Netherlands, a position held since 2025. Previously, they were a Study Director at Charles River Laboratories, where they co-led preclinical toxicology studies, ensuring compliance with GLP regulations while managing multi-disciplinary teams. With experience as a Senior Scientist at the MERLN Institute for Technology-Inspired Regenerative Medicine, Laury specialized in synthetic embryology and data interpretation. They began their research career as a Young Researcher at Universidad Industrial de Santander, developing molecular biology protocols. Laury holds a Bachelor’s Degree in Biology from the same institution and is currently pursuing a PhD in Biomedical Science at Radboud University.