Institutional Review Board at CSU

Contact IRB

Please do not hesitate to contact us with questions or concerns about human research issues, or for assistance or advice in preparing approval request forms.

Research Integrity & Compliance Review Office
(970) 491-1553
Ricro_Information_Reply@mail.colostate.edu

IRB Chairs

Matt Hickey, Ph.D.
Biomedical IRB Chair, University Distinguished Teaching Scholar, Graduate Program Director
Professor Health & Exercise Science
(970) 491-5727
Matthew.Hickey@colostate.edu

Gene Gloeckner, Ph.D.
Social, Behavioral, and Educational Research (SBER) Chair
Professor School of Education
(970) 491-7661
Gene.Glockner@colostate.edu

IRB Staff

Evelyn Swiss, CIP
SBER IRB Coordinator
Lead SBER Coordinator
(970) 491-1381
evelyn.swiss@colostate.edu

Tammy Felton-Noyle, CIP, CCRP
BMR IRB Coordinator
Lead Biomedical Coordinator
(970) 491-1655
Tammy.felton-noyle@colostate.edu

About IRB

The University is required to comply with the federal regulations governing review of research that involves human subjects (see the IRB Human Subjects Policy). Annually we must assure the Office for Human Research Protections (OHRP) that the University is complying with the requirements of 45 CFR 46. This is an NIH reference, but has been incorporated virtually verbatim into the regulations of 16 other federal agencies; additionally, the regulations state that the University will apply the same standards to all projects involving human subjects, regardless of funding or funding source. Activities are to be reviewed as proposals, and may not wait until funding for the activity is forthcoming.

45 CFR 46 includes two definitions critical to identifying whether a project must be reviewed:

Research:

A systematic investigation (i.e. the gathering and analysis of information) designed to develop or contribute to generalizable knowledge. (46.102(d)) For more information, view Is My Project Research?

Human Subject:

Individuals whose physiologic or behavioral characteristics or responses are the object of a study in a research project. Under the federal regulations human subjects are defined as: living individual(s) about whom an investigator conducting research obtains: (1) data through intervention or interaction with the individual; or (2) identifiable private information. (46.102(f)) For more information, view Does My Project Involve “Human Subjects”?

The regulations then necessarily apply to evaluations, providing services, demonstration projects, and other activities not typically thought of as “research.” They are systematic collecting of data and they, by virtue of publication, public presentation, thesis, dissertation, or project report, contribute to generalizable knowledge. It is immaterial whether the project is funded by commercial entities, funded by governmental agencies, or unfunded. Any activity involving human subjects is subject to review, including soliciting questionnaires and surveys, videotaping activities, audio taping, observing behavior, and obtaining individually identifiable data about a person.

The Institutional Review Board and its Membership

Committee members must be familiar with the diverse regulations, including those of the Health and Human Services, the Food and Drug Administration, the Department of Education, and the State of Colorado. They must be current on recent interpretations of the regulations from the federal Office for Human Research Protections (OHRP) and elsewhere. The federal regulations specify the minimum requirements for membership at §45 CFR 46.107.

Although they each represent their own academic expertise, they are committees of the institution and must reflect community and institutional values and standards. Committee members devote 7-12 hours per month, 12 months per year, to IRB meetings and protocol reviews; the IRB Chairs are involved in an additional 25 hours or more per month reviewing responses and protocols, discussions with researchers, and problem resolution. Membership on the IRB is a service responsibility; members are not paid. The Research Integrity & Compliance Review Office (RICRO) serves as the administrative support unit for the IRB, acting on behalf of the Committees and serving as a consistent contact point and resource for information.

IRB members serve a three-year term, which may be renewed. New members are nominated by the IRB and appointed by the Vice President for Research in consultation with the Deans of the colleges conducting human research and the involved Department Heads/Chairs. The University’s Bioethicist is a permanent appointment. The rosters of the IRB are approved by OHRP to verify the committee is consistent with the intent of the federal regulations. Normally new members join at the start of the University’s new fiscal year, in July.

The membership as of July 2018 is as follows:

Biomedical (BMR) IRB
Matthew Hickey, Ph.D.
491-5727
Regular Member, Professor, Chair of the BMR IRB Department of Health and Exercise Science
Bruce Cooper, M.D. Regular member, Physician, Community representative Medical Director Health District of Northern Larimer County
Tammy Felton-Noyle, CIP, CCRP Regular member, Scientific RICRO
Steve Matthews, M.D. Regular member, Physician Hartshorn Health, CSU
Ketul Popat, Ph.D. Regular member, Associate Professor, Scientific Mechanical Engineering Department
Bernard Rollin, Ph.D. Permanent Member, Professor, Non-scientist Philosophy Department
Kimberly Cox-York, Ph.D. Alternate Member, Instructor, Scientific Food Science and Human Nutrition
Susan Gloeckner Alternate Member, Non-Scientific HDS Technology
Kirk McGilvray, Ph.D. Alternate Member, Research Scientist/Scholar, Scientific Mechanical Engineering Department
Jennifer Peel, Ph.D. Alternate Member, Associate Professor, Scientific Environmental and Radiological Health Sciences
Social, Behavioral, and Educational Research (SBER) IRB
Matthew Rhodes, Ph.D. Regular member, Professor, Chair of the SBER IRB, Scientific Psychology Department
Gene Gloeckner, Ph.D. Regular member, Professor, Associate SBER IRB Chair, Social Scientist School of Education
Moti Gorin, Ph.D. Regular member, Assistant Professor, Non-Scientific Philosophy Department
Joel Painter, MSW Regular member, Non-Scientific, Prisoner Representative, Community Representative Jacob Center
Evelyn Swiss, CIP Regular member, Non-Scientific RICRO
David Williams, JD Regular member, Non-Scientific Department of Philosophy
Claire Calhoun, CIP Alternate Member, Scientific Export Control
James Folkstad, Ph.D. Alternate Member, Professor, Scientific School of Education
Elizabeth Hicks, BS Alternate Member, Scientific Community Member
Olivia Kail, BA Alternate member, Non-Scientific Student Representative
Daniel Lennox Alternate member, Scientific Student Representative, Computer Science
Sarah Olson, MA Alternate member, Non-Scientific International Programs

View a printable version of the IRB Membership.

Committee Statistics

Type of Review Average Days to Approve Number of Current Active Protocols Number of Amendments
Expedited Review 33 578 263
Full Committee Review 38
Amendments by Expedited Review 7
Exempt Review 15 295

6 Month period from June 30th, 2013 – December 31st, 2013; Number of days are Calendar days

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