Human Subjects Research at Duke

DOCR approval will not be given for a study in the eIRB until everyone on the key personnel list has successfully completed this (instructor-led or online) training. This training is designed to provide new employees in the clinical research community information about regulations, guidelines, and policies for conducting clinical research at Duke University. This course is an overview of the complex regulatory environment of human subjects research. It examines the various types of human subjects research, identifies study team roles and responsibilities, and provides an overview of Duke¿s clinical research structure. Register for this course in the Duke LMS.