Clinical research coordinators are responsible for overseeing the daily activities of the staff conducting the research. They work with principal investigators to determine if study is viable and figure out a budget. They also review the protocol of the research, ensure test subjects are familiar with that protocol, and help conduct research.
Clinical Research Coordinator Tasks
Compile, organize and submit institutional review board documentation.
Obtain and maintain informed consent of research subjects or their guardians.
Handle and review clinical trial processes and ethics compliance.
Report side effects and safety findings from drug trials or testing.