This course is designed to provide a comprehensive introduction to the field of clinical research. Participants will learn about the key concepts and principles of clinical trials, including Good Clinical Practice (GCP), clinical trial design, study conduct, data management, and regulatory compliance. The course will also cover practical skills in study coordination, site management, data analysis, and report writing.Objectives:Upon completion of this course, participants will be able to:Describe the purpose and process of clinical research and clinical trials.Explain the principles of Good Clinical Practice (GCP) and regulatory compliance.Design a clinical trial protocol and implement a study according to the protocol.Manage clinical trial sites and coordinate study activities.Analyze and interpret clinical trial data.

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