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

Virtual Concierge

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Virtual Concierge

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AAHRPP Accredited
since 2009


Office of Clinical Research

COVID-19 Research FAQs COVID Screening Questionnaire
Home Visits SOP Forum Slides
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


forum graphic Research Forums will be offered the
4th Thursday of each month
from 1:00 pm – 2:00 pm.

To reserve your virtual seat, visit the
VPR’s Virtual Meeting Scheduler and complete the REDCap survey.

View slides from previous forums


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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.