• 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 ...