Clinical Research Coordinator or Monitor

I am very enthusiastic about beginning a career in clinical research. As you can see I have no direct experience in this field, however, my father was in a clinical trial study at Emory University for his prostrate cancer. I followed his participation in the study and was involved in his care during this time. In addition, as a home health care nurse, I treated several patients that were also involved in clinical trials in Phase I and Phase II. If hired, I would work hard to see that all federal and company policies were followed and that patient's were well informed in their consent process /IRB. I would read and know the Protocols for each study as well as knowing the Investigator's Brochure. Working as a team player I would gather data in a timely and organized manner being careful to ensure that no adverse affects were being left out. Which would also mean fewer queries being sent from the team. Thru diplomacy I would take a proactive approach to clear up issues as they arise. Being available for both the site and company as a competent resource. In closing, I would also like to remind you that my past experience as a teacher will be an asset as the need to train others may arise. I hope that I will hear from you soon! Thanks, Kandee Parker, RN

Clinical Research

Isle Of Palms, SC