Lisa Chan

 Director of Clinical Affairs

Lisa Chan is a certified PMP, Scrum Master and holds a master’s degree from National Taiwan University (Molecular and Cellular Biology). Lisa has vast experience in clinical trial management and regulatory submissions with over 20 studies in various indications, ranging from new drug to medical devices studies. Prior to joining AIBEDA, Lisa served as Medical Affairs Lead, Project Manager, Contract Management Specialist and Clinical Research Associate in software, biotechnology, and global pharmaceutical companies.