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Lyette Richards is a Clinical Trial Manager and Consultant who has worked in various pharmaceutical companies over the years. With a background in Clinical Pharmacology and a strong focus on protocol development and study management, Lyette has extensive experience in writing protocols, conducting site visits, overseeing study progress, engaging with vendors, and preparing reports for submission to regulatory authorities. From Assistant Director of Phase 1 Clinical Trials to Clinical Research Associate, Lyette's expertise and skills have been honed through years of experience in the pharmaceutical industry.