HRPP

Information for Research Participants

A Guide to Participation in Clinical Research Studies

This guide, authorized by the Institutional Review Board (IRB) of the University of Cincinnati, was written to help people decide whether or not to enter a clinical or drug research study. This guide will also explain the basic information about clinical or drug research studies.

Click here for the full guide:  Guide to Participation in a Research Study

Other Useful Information for Research Participants

UCHealth Clinical Trials
Veterans Affairs Clinical Trials
Cincinnati Children's Hospital Clinical Trials
National Cancer Institute
NetWellness
HIPAA Information for Participants
Why Volunteer (pamphlet)

National Cancer Institute: Donating Your Tissue for Research

 

Contact Us


Human Research Protection Program
(ML0567)
University Hall, Suite 300
51 Goodman Drive
PO Box 210567
Cincinnati, OH 45221-0567
General Inquiries:
513-558-5259
irb@ucmail.uc.edu

Click here to identify the person dedicated to serving your research group

 

Angela Braggs-Brown, RAC, CIP, MA
Director
513-558-3005
angela.braggs-brown@uc.edu

Kareemah Mills, CIP
Assistant Director
513-558-3576
kareemah.mills@uc.edu

Claudia Norman, CIP
Education and Outreach Specialist
513-558-5784
claudia.norman@uc.edu

Human Protection Administrators

Laura Goins
513-558-0479
laura.goins@uc.edu

Martina Harmon, MS
513-558-1881
martina.harmon@uc.edu

Tara Knipp, CIP
513-558-3731
tara.knipp@uc.edu

Christa Preston, CIP
513-558-2087
christa.preston@uc.edu

Deborah Quinones-Stewart
513-558-6915
deborah.quinones-stewart@uc.edu

Quality Assurance Auditors
Jackie Glass, CCRP
513-558-0453
jacklyn.glass@uc.edu

Brianna Mills
513-558-2286
brianna.mills@uc.edu

StrokeNet CIRB
Susan Roll, RN, BSN, CCRP
CIRB Liaison
513-558-6061
susan.roll@uc.edu

Jo Ann Behrle
Human Protection Administrator
513-558-5273
joann.behrle@uc.edu

Keeley Lynch
CIRB Coordinator
513-558-5209
keeley.lynch@uc.edu