About me
As the Sr. Director of Regulatory Capabilities and Submissions at Eli Lilly, I am responsible for ensuring functional proficiency in regulatory medical writing. Leveraging my medical training at the USC Keck School of Medicine, and regulatory training and experience in clinical trial management and data reporting, I am integrating business processes and translating content requirements into scalable solutions and technology. Prior to Lilly, I worked at the Department of Defense and USC School of Pharmacy, specializing in drug development, preclinical and clinical testing of drugs, vaccines and diagnostics and regulatory submissions.
