Responsibilities: Coordinate clinical research studies. Recruit and enroll participants, ensuring consent. Manage and ensure data accuracy. Ensure regulatory compliance and document submission. Facilitate communication among stakeholders. Monitor and maintain quality assurance. Prepare documentation and assist in reporting. Provide training and stay updated on industry trends. Qualifications: Bachelor's or Master’s degree in a relevant field. Previous clinical research experience preferred. Knowledge of GCP guidelines and regulatory requirements. Strong organizational and communication skills. Proficient in Microsoft Office and clinical trial management systems.