PhD Virtual Info Session – Medpace Belgium

Coordinate study activities between internal teams, sponsors, sites, and vendors while overseeing supply management and quality reviews within the Trial Master File. Collect essential documents for patient screening, organize regulatory start-up submissions to Institutional Review Boards, and communicate with medical staff at clinical research sites. This virtual info session covers these responsibilities for Associate Clinical Trial Managers, Clinical Research Associates, and Regulatory Submissions Coordinators, with pre-screening followed by a Teams event on September 22 at 11:00 AM.