About OHRP Education & Training

The mission of the OHRP Education & Training program is to develop and implement training initiatives that will provide guidance and information on the ethical and regulatory issues related to protecting human subjects involved in biomedical and social/behavioral research.

The goal is to provide current information and resources to research team members to facilitate the successful conduct of their studies. The training initiatives are designed to meet the specific needs of research team members.

OHRP Monthly Training Opportunities

Each month, the Office of Human Research Protection offers free training sessions on various topics, some of which include Informed Consent Documents;  Adverse Events; Continual Review; and Amendments.  For session descriptions and the training calendar, select the link below:

OHRP Monthly Training Sessions

OCIS Monthly Training Opportunities

The Office of Clinical Investigative Services is offering a training series called "Taking the Mystery Out of Clinical Research Finances".  Sessions will be offered on topics that include Clinical Research Scheduling and Billing; Study Contracts; How to Create a Study Budget;  Billing Insurance, plus several more.  For more information, see the link below:

Clinical Research Finance Training Sessions

Select the below link for a training requirements checklist:

Checklist of Training Requirements for Conducting Human Subjects Research

If you have any questions or need assistance, please contact:

Kim Koss, BA
Clinical Research Training Coordinator
706-721-1481 (office)
706-721-1479 (fax)

kkoss@mcg.edu