GETTING STARTED....
REQUIRED TRAINING AND CREDENTIALING

Human Subjects Research Education Program - IRB Certification for Emory University Clinical Research Faculty and Staff. Read more>>

HIPAA Training for Emory University Faculty and Staff. Read more>>

IATA Safe Packaging and Shipping of Clinical Specimens. Read more>>

Emory Healthcare Credentialing for Non-MD Emory University Clinical Research Staff. Read more>>

JOIN OUR LISTSERV: Email us with your Emory email address and we'll get you added so that you can keep up with events, announcements, etc.

ABOUT US

The Emory University School of Medicine Office for Clinical Research (OCR) exists to ensure leading-edge, efficient clinical research investigations, yielding improved patient care and outcomes. OCR is part of the Emory University School of Medicine (EUSOM) Office of Research Administration.

OUR MISSION

Guided by the highest ethical and research standards, the mission of the OCR is to organize and enhance operational processes that support the efforts of the clinical research team and to facilitate the timely initiation, execution, management and completion of clinical trials at Emory.

NEWS BULLETIN :

MANDATORY use of Pharmacy Services for Management of Investigational Drugs. Read more >>

MANDATORY review required for all new clinical trials and certain other new research studies involving human subjects on behalf of Dean Lawley and Dr. David Stephens. Read more >>

WHAT'S NEW:

Request for Coverage Analysis Cover Sheet found under "Forms" link

Federal and Non-Federal Investigator Effort Calculation Reports found under "Protocol Routing Pathways" link

Thinking of Volunteering for a Clinical Trial?

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