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Course Description

This program is designed for physicians transitioning into the role of principal investigator and/or sub investigator within the research industry.
Upon completion of this course, clinicians will be competent and gain the valuable skills needed
in order to conduct a well-organized and controlled clinical research study within their institution and/or
private practices.

Who is the target audience?

Physicians interested in the domain of clinical research

What am I going to get from this course?

· Understand the general process of clinical trial
· Understand the role of the Investigator/ sub-investigator in clinical research
· Understand the importance and the process of the informed consent
· Identify the clinical trial documents and their role in the clinical trial process
· Understanding the consequences of non-compliance and fraud in clinical trial
· Describe the elements of a protocol including the hypothesis, objectives, endpoints,
  and inclusion/exclusion criteria, as well as its corresponding CRF