The University of Arizona

Participants' Bill of Rights

Report Misconduct

Ethics Hotline

HSPP Contacts

VPR-IRB@email.arizona.edu

Mariette Marsh, Director
(520) 626-7575

Andi Encinas, IRB Manager
(520) 626-8630

Liz Baldry, IRB Associate
(520) 626-0256

Mason Burchfield, IRB Associate
(520) 626-0433

Gina Fimbres, IRB Associate
(520) 626-0026

Christine Melton-Lopez, IRB Coordinator
(520) 626-5859

Courtney Olson, IRB Associate
(520) 626-1744

Darlene Villicana, IRB Associate
(520) 626-6282

Street Address
1618 E. Helen Street
Tucson, AZ 85721

Mailing Address
POB 210409
Tucson, AZ 85721


HOW ARE WE DOING?

Customer Service Survey


 

Whether you volunteer to participate in a research protocol as a healthy participant or as a patient, you have certain rights. At the University of Arizona, we believe that personal concern for every study volunteer is indispensable to the quest for knowledge. The most important person in research is the participant. The participant is the essential element without which research could not be conducted or response to intervention measured.

  • As a study participant, you have the right to considerate and respectful treatment; before, during and after your participation ends. As part of that respect, you have a right to know what the study is about and what you will be asked to do during your participation in the study.
  • It is important that you know all options in order to freely choose whether to participate in a research study.
  • If at any time you wish to withdraw from a research study you have the right to do so. If you have received medical intervention during your participation you have the right to be informed of the medical consequences of your withdrawal.
  • As a participant, you may have questions even after you have given your consent. Please do not hesitate to discuss these questions with the Principal Investigator or research personnel. It is important for you to understand exactly what the study is about and why.
  • You are entitled to receive a copy of the consent form you signed. Ask for this when you sign the consent form.
  • It is important that you be aware of any risks from your participation and understand how the research may affect you.
  • It is important for you to know about any benefits that you might receive from your participation.
  • When there are alternatives to therapeutically designed research protocols, you have the right to know about them.
  • You have the right to refuse to participate in research.
  • You have the right to privacy concerning the information that is obtained for research purposes.
  • You have the right to be told whether there are any costs associated with your participation and whether you will be compensated for participating in the study.
  • You have the right to expect that all communications and records pertaining to the research will be treated as confidential to the extent permitted by law.
  • You have the right to be told who to contact with questions about the research, about research-related injury, and about your rights as a research participant and to be given information regarding available treatment should you have a research-related injury.