Lisa Barry is a Clinical Study Lead at Regeneron, drawing upon a wealth of experience in clinical project management and scientific research. They have held roles including Clinical Trial Project Manager at Eli Lilly and Company, where they led cross-functional teams in oncology trials, and Pharmacovigilance Operations Specialist at IQVIA, focusing on patient safety data. Lisa’s academic background includes an honours degree in Microbiology from the National University of Ireland, Galway. Known for their ability to build rapport with diverse stakeholders and maintain high-quality standards, they are committed to advancing healthcare product development.
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