Job descriptionTrial management : Coordinate all aspects of clinical trials, from startup to closeout, ensuring adherence to protocols and timelines.Participant management : Recruit, screen, and enroll eligible participants; obtain informed consent; and monitor participant safety and compliance throughout the study.Data management : Collect, enter, and validate clinical trial data, ensuring accuracy and completeness. Generate reports and maintain study-related documentation, including case report forms and other regulatory forms.Regulatory compliance : Ensure all trial activities comply with relevant regulations, Good Clinical Practice (GCP), and ethical guidelines. Prepare and submit documents to the Institutional Review Board (IRB).Liaison and communication : Act as a point of contact for investigators, sponsors, laboratories, and regulatory bodies.