Research Participant Advocacy Program

The Research Participant Advocacy Program provides consulting expertise on human subjects and regulatory issues, including IRB applications, the informed consent process, study feasibility and good clinical practice (GCP). Contact us for quick expert help.

The Research Participant Advocates serve as a resource to research teams and research participants

The Research Participant Advocates review applications to the Clinical Research Unit to assure high standards for Human Subjects Protections. Call us to review your consent form, protocol or data and safety monitoring plan. Let us help you to prepare the best possible research plan.

The Research Participant Advocates are a training resource to investigators and their staff. Want to know how to administer the best consent? Do you need help with Good Clinical Practice (GCP’s)? Do you need to know how to report an unanticipated study event?  Do you have to assemble a Data Safety Monitoring Plan and don’t know how to do it?  The RPAs can help you with these and more.

The Research Participant Advocates serve as a resource to volunteers.   Contact us for an independent witness to the consent process, to serve on the volunteers’ behalf in the case of a misunderstanding between the volunteer and study team, or to provide information about research in general or a specific protocol.