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Helene Lake-Bullock Director/Research Compliance Officer
Pam Stafford Associate Director/QA/QI Program
Suzanne Arnold Medical IRB #6 Full Review/RDRC
Sam Bell Medical IRB #1 Full Review
Joe Brown Research Privacy Specialist (HIPAA)/Exempt Review/IRB Reliance Manager
Jeeyoung Chun Education Instructional Designer
Elisa Crill Nonmedical IRB #4 Full & Expedited Review
Katie Gieske Nonmedical IRB #4 Full & Expedited Review
Gregory Hatton IRB Reliance
Joanne Hines Medical IRB #2 Expedited Review
Erin Hoff QA/QI Program (Lead/Internal)/Research Education Support
Matthew Howell IRB Reliance/QA/QI Program/Research Education Support
Jennifer Kearns Medical IRB #1 & #2 Support
Susan Keefer Nonmedical IRB #4 Support/Research Education Support
Judi Kuhl E-IRB System Administrator
Karen Larson Medical IRB #3 Expedited Review
Jill Marion Medical IRB #1 Expedited Review
TBD Medical IRB #2 Full Review
Emily Matuszak Responsible Conduct of Research (RCR), QA/QI
Olga Moskalyuk Medical IRB #3 & #6 Support
Desiree Penn Assistant to Director/IRB Support/Research Education
Beverly Raisor Medical IRB #3 Full Review
Lindsay Schneider Medical Exempt Review
Belinda Smith Research Education Specialist/FDA-Regulated Research
Jenny Smith Responsible Conduct of Research (RCR) Education/UK LabArchives Team/Research Privacy Concerns
Kimberly Williams Nonmedical Exempt Review

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Additional Contacts

IRB Protocol Questions E-mail: IRBSubmission@uky.edu
E-IRB Technical Support Email: EIRBsupport@uky.edu
IRB Reliance Email: IRBReliance@uky.edu
Human Subject Protection Training Email: HSPTrainingSupport@uky.edu

Concerns, Suggestions, or Questions

ORI/IRB Administrative Procedures

In accordance with the Office of Research Integrity (ORI) and the Institutional Review Boards' (IRB) commitment to continuous improvement in its policies, practices and procedures, there is a process to formally register suggestions, concerns and/or complaints regarding the ORI and/or the IRB administrative procedures.  Issues raised will be resolved as quickly, fairly and amicably as possible through cooperative exchange of information.  

Concerns, suggestions, or questions regarding the ORI and IRB administrative procedures should be filed with the Director of ORI, Helene Lake-Bullock, who will evaluate and investigate the concerns raised and determine what actions, if any, should be taken by the ORI, IRB and/or the investigator to address the issue.  Helene Lake-Bullock may be contacted by phone (859) 257-9428 or email hlbullo@uky.edu.

Concerns, suggestions, or questions regarding the ORI and IRB administrative procedures that cannot be resolved at the level of the Director of the ORI will be forwarded to the Vice President for Research, who shall be the final deciding body. 

IRB Members

Concerns regarding attempts of undue influence on individuals responsible for the oversight of human subjects research should be reported to the Research Compliance Officer (RCO) who notifies the Vice President for Research (VPR) and the Director of ORI, Helene Lake-Bullock. The VPR, in consultation with the ORI Director, determines the appropriate response to unduly influence or undermine the mission of the IRB. The RCO, Helene Lake-Bullock, may be contacted by phone (859) 257-9428 or email hlbullo@uky.edu.

Investigator Concerns About IRB Decisions

Concerns, suggestions, or questions raised by a Principal Investigator regarding a specific IRB submission or decision should be resolved by direct communication between the investigator and the IRB committee (see Initial Full Review SOP, Expedited Review SOP, Exempt Review SOP, and/or Noncompliance SOP).

Subject Concerns, Suggestions, or Questions

It is IRB policy that a safe confidential, and reliable channel for current, prospective, or past research participants, their representatives or others, is provided that permits them to discuss problems, concerns, and questions; obtain information; or offer input with an informed individual who is unaffiliated with the specific research protocol.

IRB approved informed consent documents for U.S. based studies include the ORI Research Compliance Officer's toll-free phone number (1-866-400-9428) as a subject's primary contact point for this purpose. Contacts listed in the informed consent documents for international or non-English speaking populations are determined on a case-by-case basis.

Submit Feedback Online

For your convenience, you have the option to submit feedback anonymously using ORI's online customer service form.

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