Sara Cummins is a seasoned regulatory affairs manager with over 17 years of experience in the pharmaceutical industry. Currently serving as a Sr. Advisor in Global Regulatory Affairs CMC at Eli Lilly and Company, they are responsible for the submission strategy and coordination of Lilly's biologic portfolio to global regulatory authorities. Previously, Sara held roles at Pfizer, SIGA Technologies, and Sandoz, where they excelled in regulatory strategies and submission preparation for various pharmaceutical products. They earned a MS in Integrative Pharmacology from Michigan State University and a Bachelor's degree in Pharmaceutical Sciences from Purdue University.
Location
Corvallis, United States
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