Role Description
Clinical Research Coordinator Coordinate and manage clinical trials and research studies from initiation to completion Ensure study protocols are followed in compliance with regulatory requirements (GCP, IRB, ethics standards) Recruit, screen, and enroll eligible study participants Obtain informed consent and maintain participant documentation and records Schedule and coordinate patient visits, assessments, and follow-up procedures Collect, manage, and validate clinical trial data for accuracy and completeness Liaise with investigators, sponsors, hospitals, and regulatory bodies Monitor study progress, timelines, and protocol adherence Ensure patient safety and report adverse events or protocol deviations Support audit preparation and regulatory inspections Biomedical Research Analyst Conduct scientific and biomedical research using laboratory and clinical data Analyze biological, medical, and experimental data using statistical and computational tools Support devel...