Clinical research plays a pivotal role in the development of new medical treatments and interventions, and CRCs are at the heart of this process, managing the day-to-day operations of clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. The course covers a wide range of topics, including the fundamental principles of clinical research, the intricacies of planning and preparing for trials, the roles and responsibilities of CRCs, and the ethical and regulatory considerations that underpin clinical studies. Participants will gain hands-on experience in protocol development, site selection, budget management, and contract negotiation, while also exploring advanced topics such as data management, patient recruitment, and quality control. By the end of the course, attendees will be well-prepared to take on the challenges of coordinating clinical trials and contribute to the advancement of medical science and patient care. Participants will also delve into the critical aspects of stakeholder communication, ensuring effective collaboration with investigators, sponsors, and regulatory bodies. The course emphasizes the importance of ethical considerations, highlighting historical case studies and current best practices to ensure participant welfare and data integrity. Through interactive activities and real-world case studies, learners will develop the problem-solving and decision-making skills essential for navigating the complexities of clinical research. This comprehensive training will empower participants with the knowledge and practical skills necessary to excel as Clinical Research Coordinators, driving innovation and enhancing the quality of clinical trials.