Clinical research coordinators and other study staff members tasked with obtaining informed consent from research participants are invited to complete a 10- minute survey for a study about the informed consent process.
The purpose of the study is to survey those who are responsible for obtaining informed consent from prospective research participants to get their perspective on the biggest challenges they face when explaining research studies to potential participants.
If you are 18 years or older and a member of a research team who is currently, or has been previously, responsible for obtaining informed consent from prospective research participants, you are eligible to participate.
If you participate, you will be asked to complete a brief, anonymous online survey of your experiences obtaining informed consent from research participants. It should take no more than 10 minutes to complete. You can access the survey here.
Your participation is completely voluntary, and your responses will be anonymous and not linked to any identifying information.
If you have any questions, please email the student investigator at firstname.lastname@example.org.