Engages learners in the concepts and principles of implementing and conducting clinical trials of drugs or devices. Examines the key components of good clinical practice when conducting and documenting clinical trials. Emphasizes the key roles of the research assistant/coordinator when engaging with research participants, the other members of the research team, the participants' clinical team, and other internal and external entities involved in clinical trial conduct. Offers learners an opportunity to develop necessary skills to apply ethical principles, implementation strategies, safety monitoring, and source documentation requirements when serving as a research assistant/coordinator for a clinical trial. Designed for healthcare professionals who are interested in participating on a research team conducting a clinical trial.