Parvin Perrino

Senior Director, Regulatory Affairs Clinical/nonclinical; Global Regulatory Lead

Parvin Perrino is an experienced professional in regulatory affairs, currently serving as Senior Director of Regulatory Affairs Clinical/Nonclinical and Global Regulatory Lead at BioMarin Pharmaceutical Inc. since June 2013. Prior roles include Senior Director, Regulatory Affairs Labeling and various positions in regulatory affairs focusing on labeling. Perrino's extensive background includes experience at Amgen as Manager of Regulatory Affairs Promotion and Senior Associate in Global Labeling. Additional experience includes a contract position at Kforce Inc. supporting Amgen, an internship at Regeneron Pharmaceuticals, and research assistance at Brentwood Biomedical Research. Educational qualifications include a Master's degree in Bioscience with a focus on Clinical and Regulatory Affairs from the Keck Graduate Institute and a Bachelor's degree in Biochemistry from UCLA.

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