Cecile RiboudSenior Director Europe Integrated Global Compliance at IQVIA
Cecile is currently responsible for IQVIA’s Integrated Global Compliance in Europe, designing solutions for safety, regulatory and quality compliance. She has over 17 years of life sciences experience across Scientific Information Management, Global Regulatory Affairs and support for Mergers and Acquisitions. Having worked for pharmaceutical groups and consulting and technology companies in Europe, Cecile has an excellent understanding of the pharmaceutical and MD-IVD industry. She has held global leadership positions, leading large global programs and teams of experts. Prior to joining IQVIA, Cecile worked at a well-known regulatory consulting firm in Germany, where she served as acting deputy head of an office totaling 60 regulatory consultants and led global projects involving 70 regulatory consultants worldwide. She was responsible for client delivery of Regulatory Outsourcing Programs. During her career she led regulatory and clinical workstreams of company integration and portfolio acquisition & divestment projects, for a total of over 20,000 licenses transferred. Cecile holds an M.Sc. in Analytical Sciences from the University of Strasbourg, France and an Executive MBA from EMLyon Business School, France – Shanghai, China.