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The Research Subject Advocates' Role at the GCRC
 Our goal is to ensure that all participants have a full understanding of what clinical research is, the risks involved, and their rights as study volunteers. We are also available to serve as unbiased observers during the informed consent process, and we will work on the participants' behalf to protect their rights at any point before, during, or after their participation.
All GCRC research participants are encouraged to contact the RSA team (information below) with concerns regarding safety or informed consent.
David Badesch, MD
Research Subject Advocate
(303)315-1805
Barbara Hammack, PhD
Research Subject Advocate
(303)372-8810
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