"In my previous position, I did not feel like the patients had a clear understanding of the complex research protocols. In my opinion, the previous CRC did not explain the informed consent process very well at a level the patients could understand. When I was hired, I developed guidelines on how to inform the patients at a level they could understand to increase their safety. Once the patients had a clear understanding of the protocols, I felt they were more capable of making an informed decision."

Clinical Research Coordinators are exposed to vital patient information. They need to keep the patient's health information secure while screening patients to be sure they fit the guidelines of the trial. Describe measures you have taken to increase the safety of your patients. The interviewer wants to hear that the safety of your patients is your primary concern.