/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: ShinjitaGhosh https://cdn.slidesharecdn.com/profile-photo-ShinjitaGhosh-48x48.jpg?cb=1523660960 • Exposure in the field of clinical trial (Phase III and Phase IV studies) and various kinds of academic projects. • Management of internal EC meeting, dossier handing and coordinating with sponsor and PI for closing the necessary queries and approval of the study. • Developed and implemented informed consent documentation guidelines. • Worked closely with clinical trial sponsors for site assessment, qualification and initiation visit& Schedule and participate in monitoring activities • Conduct independent study coordination and screen potential patients for protocol eligibility& oversaw and implemented daily operational aspects of clinical research • Ensured research protocol compliance ...