Clinical Research Associate (CRA) course provides comprehensive training in clinical trial processes, regulatory guidelines, and Good Clinical Practice (GCP). The curriculum covers study design, protocol development, site selection, monitoring visits, and data management. Students learn ethical considerations, informed consent procedures, and safety reporting. Emphasis is placed on ICH-GCP, FDA, and global regulatory requirements. Practical modules include case studies, documentation, and site communication. Designed for aspiring CRAs, this course equips learners with essential skills to monitor clinical trials, ensure compliance, and support drug development. By the end, participants are prepared for roles in clinical operations within pharmaceutical and research organizations.