About this Course
This course focuses on the work of carrying out a clinical trial. We’ll cover the complex work of preparing for a study, as well as the myriad details that control its conduct.
What You'll Learn
- Creation of the protocol, case report forms and consent forms
- Approaches to prepare for clinical studies
- Issues related to participants in a clinical study and their roles/obligations (subjects, investigators, sponsors, clinicians, etc.)
- Site selection, initiation and ongoing management
- Study initiation procedures
- Data management principles and practices