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Geraldine Moune is a seasoned professional with extensive experience in regulatory affairs and site activation within the clinical research industry. Currently serving as Vice President of Regulatory Affairs and Senior Director of Site Activation Therapeutic Lead at Worldwide Clinical Trials since March 2012, Geraldine Moune has a proven track record of providing strategic leadership, ensuring compliance with global regulatory requirements, and managing cross-functional teams and resources. Previous roles at PharmaNet/I3 and Pierre Fabre include overseeing regulatory affairs across the EMEA region and managing project-related regulatory issues. Geraldine Moune holds a Master’s degree in International Development and Registration of Drugs from Paris-Sud University and a PharmD from Université Paul Sabatier Toulouse III.