Course overview
Building on knowledge gained in earlier clinical trials courses, this course will focus on the practical aspects of clinical trial conduct and aligns with the program intent to provide fundamental concepts and principles including activities that promote professional development in clinical trials. Students will gain relevant training in planning and implementation of clinical trials, including a more in-depth understanding of regulations, as well as learn practical aspects of informed consent and adverse event documentation
- Clinical trial design
- Ethics and regulation
- Safety and efficacy
Course learning outcomes
- Critically apply the principles governing the conduct of clinical trials
- Interpret and implement a clinical trial protocol from a site and contract research organization perspective
- Articulate critical aspects of informed consent in the clinical research setting
- Articulate critical aspects of adverse event documentation in clinical research setting
Degree list
The following degrees include this course