Lisa Chang

Lisa Chang, RAC, is a seasoned regulatory affairs professional currently serving as Senior Manager Regulatory Affairs at Travere Therapeutics since April 2020, following a tenure as Regulatory Affairs Manager at Polaris Pharmaceuticals. With extensive experience in managing regulatory submissions for Phase I to III clinical trials across multiple countries, Lisa has demonstrated expertise in global safety and regulatory requirements, training new associates, and ensuring compliance with FDA guidance. Previous roles include positions at HUYA Bioscience International, where Lisa contributed to regulatory submissions and translation efforts, and independent research roles at UC San Diego. Lisa holds multiple certificates in Clinical Trials Design and Management and Biostatistics, as well as a BS in Biochemistry/Chemistry.