Elizabeth Narciso

Elizabeth Narciso leads a team of regulatory operations professionals in preparing and submitting regulatory documentation on behalf of clients to the Food and Drug Administration and other health authorities. She has spent her career in regulatory operations and has integrated regulatory affairs in a variety of roles, including research associate, regulatory associate, documentation specialist, and publisher. Additionally, she has experience developing and maintaining systems and procedures. Prior to joining RPI, Ms. Narciso held roles at Genitope, PDL Biopharma, CV Therapeutics, Matrix Pharmaceutical, and Theravance. She holds a bachelor’s degree in biology with an emphasis in microbiology from San Francisco State University.