Lisa Chang, Rac
About Lisa Chang, Rac
Lisa Chang is a Senior Manager of Regulatory Affairs at Travere Therapeutics, specializing in US FDA regulations to facilitate global drug development. She has extensive experience in regulatory affairs, having held various positions at Polaris Pharmaceuticals and Travere Therapeutics, and possesses a solid scientific background in the biotech sector.
Current Role at Travere Therapeutics
Lisa Chang serves as the Senior Manager of Regulatory Affairs at Travere Therapeutics, a position she has held since 2021. In this role, she oversees regulatory strategies and ensures compliance with industry standards. Her expertise in US FDA regulations is instrumental in facilitating global drug development processes.
Previous Experience in Regulatory Affairs
Prior to her current role, Lisa held several positions at Polaris Pharmaceuticals. She worked as a Regulatory Operations Associate from 2014 to 2015 and again from 2016 to 2019, before transitioning to the role of Regulatory Affairs Manager for a six-month period in 2019. Additionally, she served as a Regulatory Affairs Manager at Travere Therapeutics from 2020 to 2021.
Educational Background and Certifications
Lisa Chang studied at the University of California, San Diego, where she earned a Bachelor of Science in Biochemistry/Chemistry from 2009 to 2013. She also completed certificates in Clinical Trials Design and Management, as well as Biostatistics, both between 2013 and 2014. Her education provides a strong foundation for her work in regulatory affairs.
Research and Translation Experience
In addition to her regulatory roles, Lisa has experience in research and scientific translation. She worked as an Independent Researcher at Pomeroy Lab, UC San Diego in 2013 and served as a Scientific Translator at HUYA Bioscience International from 2013 to 2014. These roles enhanced her understanding of scientific concepts and improved her communication skills.
Specialization in Regulatory Affairs
Lisa possesses a proven specialization in US FDA regulations, which supports her ability to navigate complex regulatory environments. Her solid scientific background complements her regulatory and clinical expertise, making her a valuable asset in the biotech sector.