Principal Investigator Education Program Clinical Research Consulting has been educating industry research professionals since 1999. Prior investigators who have participated in our program comment that our education program set us apart from the competition. It is condensed and concise and the most comprehensive in the industry, covering FDA regulations, Good Clinical Practice Guidelines, and topics that are imperative to investigators such as; informed consent, investigator responsibilities, protocol compliance, adverse events, documentation, non-compliance, fraud and FDA suspension.
Physicians work at their own pace online using our Principal Investigator Education Course. This course covers various topics critical to understanding the clinical research industry and the role of an investigator. At the end of each module, there are a series of test questions which will challenge your knowledge of the material reviewed. In addition, physicians will experience “real-life scenarios” at the end of each module where challenges, common obstacles and real life experiences are shared, relating to the specific module topics. Lastly, upon completion of the modules, physicians will participate in a final exam which will cover all of material reviewed in the course. Upon completion of our education program, test results will be provided via US Mail along with a Certificate of Completion which will document course participation and education fulfillment.
This program consists of eight modules; estimated time to complete the program is approximately 8 hours. |