Erika Mendes Correia is an experienced clinical trial manager with a strong background in clinical research and regulatory compliance. Currently serving as a Clinical Trial Manager at the Global Antibiotic R&D Partnership (GARDP) since August 2017, Erika previously held positions as a Senior Clinical Research Associate at the Drugs for Neglected Diseases initiative (DNDi) and as an Associate Clinical Site Monitor at Bristol-Myers Squibb. Erika has extensive experience in clinical monitoring processes, protocol development, regulatory submissions, and site management across various phases of clinical trials. Erika holds a Master of Business Administration from FGV - Fundação Getulio Vargas and a Licentiate degree in Biology from UERJ.
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