Jody Gould, Ph.D.
Vice President of Regulatory
Jody Gould, Ph.D. has nearly 30 years of broad experience and expertise in regulatory affairs strategy, management and policy and has supported all stages of drug and biological product development. She has managed multiple marketing applications from preparation to approval.
Prior to joining Aravive, Dr. Gould worked at GlaxoSmithKline where she contributed regulatory expertise to the development, approval, and life-cycle management of vaccines (including Shingrix) and immunotherapeutic products, as well as supported US regulatory policy and advocacy efforts. At Centocor, Inc., (now Janssen Biotech), she was the regulatory lead for multiple monoclonal antibodies for various autoimmune disorders and part of the team responsible for the initial licensure of Remicade for Crohn’s Disease. Her career began at Baxter International, where she provided CMC regulatory support for parenteral drug products.
Dr. Gould earned her M.S. and Ph.D. degrees in Chemistry from Northwestern University, and a B.S. degree in Chemistry from the University of Delaware.
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