Michelle Greenman is Vice President of Global Regulatory Affairs. She is responsible for leading the regulatory affairs team, managing regulatory operations and medical writing resources, and strategic regulatory planning for Kezar’s assets. Prior to joining Kezar in June 2020, Ms. Greenman served as Global Regulatory Lead for Retrophin (now, Travere Therapeutics). Ms. Greenman has held positions of increasing responsibility at Vital Therapies, Shire Regenerative Medicine, and Advanced BioHealing and gained experience with small molecule drug development, combination products (biologics and medical devices), advertising and promotional reviews, post-marketing commercial support and application maintenance. Most of her career in regulatory affairs has been spent working in the rare disease space.
Ms. Greenman earned her bachelor’s degree in Biology from Gustavus Adolphus College and her Doctor of Chiropractic degree from Northwestern Health Sciences University.