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Catherine Guittet joined Advicenne in 2008 and is responsible for clinical research, regulatory affairs and project management. With over fifteen years of experience in clinical affairs and regulatory matters, Catherine has held positions with Merck Serono, where she managed a unit dedicated to the coordination of early clinical development in oncology, as well as with the French biotech company, Synt:em. For several years, she served as Head of the Patient Clinical Study Unit at SGS-Aster (a contract research organization). Catherine began her career as Head of Project Management at Theraplix (Sanofi-Aventis).

Catherine received her Doctor of Pharmacy (PharmD) and PhD from Angers University, graduated as Clinical Investigator from Paris VII University, obtained a Pharmaco-Epidemiology Certificate from Bordeaux II University, as well as a Cellular Pharmacology, Pharmacogenetics and Pharmacokinetics Certificate from Paris VII University.