Explore the fundamental scientific, ethical, practical, regulatory, historical and economic principles that support successful clinical trials. Discover the major concepts guiding the design and implementation of clinical trials, and learn to project manage the numerous people and tasks involved at all stages of the process. Gain an understanding of the ethics in clinical trials from human subjects protection to data integrity, and the roles of various governing organizations. Understand the relationships between research participants, investigators, sponsors, clinicians, monitors, research coordinators and regulators.
Key Outcomes
You will be able to apply principles of good clinical trial design and management.