<ul><li>Assist in planning, organizing, and executing clinical trials in compliance with protocols, GCP, ICH guidelines, and regulatory requirements</li><li>Coordinate with investigators, sponsors, ethics committees, and study teams for smooth trial conduct</li><li>Assist in preparation and submission of study documents including protocols, informed consent forms (ICF), and case report forms (CRFs)</li><li>Screen, enroll, and follow-up with study participants as per protocol</li><li>Maintain and update clinical trial documentation, including source documents and trial master files</li><li>Ensure timely data entry, verification, and query resolution in electronic data capture (EDC) systems</li><li>Monitor patient safety by reporting adverse events (AEs) and serious adverse events (SAEs) in accordance with guidelines</li></ul>

Clinical Research