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.
Physicians interested in the domain of clinical research
· 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
