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Clinical Research Education Program

Clinical Research Consulting has been educating industry research professionals since 1999. Our prior students comment that our research programs set us apart from our competition. It is the most comprehensive in the industry, covering FDA regulations, Good Clinical Practice Guidelines, and topics that are imperative to research professionals such as; informed consent, protocol compliance, source documentation, adverse events and audits.

Students work at their own pace online using our Clinical Research Education Course. This course covers developed clinical research modules which cover various topics critical to understanding the clinical research industry. At the end of each module, there are a series of test questions which will challenge your knowledge of the material reviewed. In addition, you will experience “real-life scenarios” at the end of each module where challenges, common obstacles and real life experiences are shared with our students relating to the specific module topics. Lastly, upon completion of the modules, students 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 to the students via US Mail along with a Certificate of Completion which will document their participation and education fulfillment.

Clinical Research Education Program Testimonials

See The Agenda For This Course

This program consists of ten modules; estimated time to complete the program is approximately
10 hours.

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If you have further questions about either program, or any CRCI service, please call:
508-865-8907


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.

See The Agenda For This Course

This program consists of eight modules; estimated time
to complete the program is approximately 8 hours.

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