Office of the Vice President for Research - Research Administration

Clinical Trials


Trial Sponsor's, CRO's and External Investigators, Contact us as you look to place your clinical trial.


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OCR Concierge Services

OCR Support & Institutional Guidance

Upcoming Dates:

Nov 6, 2018 1p-4p
Nov 7, 2018 9a-12p
Nov 21, 2018 9a-12p
Dec 4, 2018 1p-4p
Dec 5, 2018 9a-12p
Dec 19, 2018 9a-12p
Jan 2, 2019 9a-12p
Jan 8, 2019 1p-4p
Jan 16, 2019 9a-12p
Jan 30, 2019 9a-12p

Learn more about
Concierge Service



AAHRPP Accredited
since 2009


Office of Clinical Research


new clinical trial submission process
Training Requirements and Opportunities
Personnel Changes
External IRB - Initial Requests External IRB - Modifications
External IRB Prompt Reporting
External IRB Inactivation Request
Clinical Trials Registration
OCR Intranet Resources


Upcoming Forum

CTO & OSP Forum:
Clinical Trial Process & Velos Data Entry
Presenters: Joseph Schmelz, PhD, Chris Green, CPA, and Jason Bates, MBA
Thursday, October 25, 2018
3:00 p.m., Long Campus - Lecture Room 409L
View Past Forums


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Latest Updates to OCR Forms & Policies

As of October 8, 2018:
updated 1.1.1 PI Responsibilites Policy
updated 1.1.3 Sponsor Investigator Policy

Make sure to always download forms from the OCR and IRB websites
to ensure you are using the most current versions!



The OCR is committed to supporting the research community in the conduct of ethical clinical research and human subject protection in compliance with the required federal, state, and local regulations. The office provides consultation on questions related to regulations and standards of practice governing human research. The OCR provides education and training; develops policy and processes; and leads quality improvement efforts in areas of clinical trial management. It endeavors to create an interdisciplinary collaborative environment among the research teams, fostering best practices.