Barbara Giglio has extensive experience in the field of pharmacovigilance and project management, currently serving as a Project Manager in the Drug and Device Patient Safety Solution at Labcorp Drug Development since April 2022. Prior to this role, Barbara has held various positions including Safety Manager at CROMSOURCE since May 2012, responsible for overseeing pharmacovigilance activities for investigational medicinal products and medical devices, and previously worked as a Materiovigilance and Pharmacovigilance Associate. Earlier experience includes a regulatory affairs role at Nuova Farmec srl, an internship at GlaxoSmithKline focused on pharmacovigilance compliance, and a research fellow position at the University of Verona, managing projects on antibody fragment development. Barbara holds a master's degree in cellular and molecular biology from Università degli Studi di Urbino Carlo Bo and a bachelor's degree in pharmaceutical biotechnology from Università degli Studi di Padova.
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