Catherine Guittet
Director of Clinical Research and Regulatory Affai
Management
Advicenne
France
Biography
Catherine Guittet, PharmD, PhD joined ADVICENNE in 2008. She is responsible for clinical research, regulatory affairs and project management. She is more especially involved in conducting Advicenne clinical trials. C Guittet has over 12 years experience in clinical and regulatory affairs. Prior to joining Advicenne, she began her career at Theraplix (Sanofi-Aventis) as Head of Project Management where she created the department. She was then responsible for early-phase and multicentre clinical trials at a top-level CRO : Aster-Cephac (SGS). She then joined Synt:em Graftys, French biotech companies, as Head of the Clinical Department. Finally, she went to Merck-Serono , where she managed a unit dedicated to the coordination of early clinical development in oncology . She has a Pharm D PhD from Angers University, graduated as Clinical Investigator from Paris VII, obtained a Pharmaco-Epidemiology Certificate from Bordeaux II University, and a Cellular Pharmacology, Pharmacogenetics and Pharmacokinetics Certificate from Paris VII University.
Research Interest
Business Development
