I am a student of the International drug development and registration master (www.adediem.com/dess_ang.asp). I chose this master to work in the pharmaceurical industry, specifically, in the Regulatory Affairs field.
Before entering this master, I was a student of the biological engineering department of the Polytechnical school of Sophia Antipolis.
My studies made me a good scientist and gave me the opportunity to have a global view of the pharmaceutical industry through courses on regulatory affairs, marketing, intelectual property and pharmacovigilance.
As I was interested in working in the international regulatory affairs, and as I lived in several countries (Kuwait, Gabon, France, Niger, Colombia, Morocco, Algeria), I decided to enter the master of international drug developement and registration.
As part of this master I am completing an internship in the Regulatory Affairs European Department of Sanofi Aventis.
FK Chebchoub
International Regulatory Affairs
Paris, France
Since 2007: European Regulatory Affairs Trainee - Sanofi Aventis |
2006 : Pharmacovigilance_Compliance Trainee - Sanofi Pasteur MSD
2005 : Research Trainee - New York University Medical Center, Department of Parasitology, New York City
2004 : Trainee - Laboratoire de Génétique et Cancer de Lyon

