Senior Director, Project Management and Regulatory Affairs
Rachel Gee provides cross functional oversight and regulatory direction to the Mycovia Pharmaceuticals team and is responsible for leading all project management and regulatory aspects of the company’s antifungal programs. With nearly 15 years of experience in the pharmaceutical industry, Ms. Gee has a diverse background in regulatory, clinical, project management, and business development roles. Ms. Gee most recently served as Director, Project Management and Regulatory Affairs at Viamet Pharmaceuticals where she was responsible for leading successful regulatory submissions and agency meetings, as well as driving the overall development timelines for multiple products within the antifungal program. She has previously served in leadership positions at a contract research organization where she led global project management departments and regulatory projects for small biotech and large pharmaceutical clients.
Ms. Gee holds a BS in Zoology from North Carolina State University and is a member of the Regulatory Affairs Professionals Society and the Project Management Institute.