Fresher Clinical Research executive

 Responsibilities:

• Create and write trial protocols, and present them to the steering committee.
• Identify, evaluate, and establish trial sites; close sites upon completion of trials.
• Train site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form (CRF) completion.
• Liaise with ethics committees to ensure the rights, safety, and well-being of trial subjects.
• Order, track, and manage Investigational Product (IP) and trial materials.
• Oversee and document IP dispensing, inventory, and reconciliation.
• Protect subjects' confidentiality, update their information, and verify that IP has been dispensed and administered according to protocol.
• Conduct regular site visits, coordinate project meetings, and write visit reports.