Sample interview questions: How do you ensure that clinical trial sites have appropriate procedures for study participant consent?
Sample answer:
- Review the site’s Institutional Review Board (IRB) or Independent Ethics Committee (IEC) approval documents to ensure that the site has obtained approval to conduct the study and that the informed consent process has been reviewed and approved.
- Check that the site has a system in place to obtain informed consent from all study participants. This may include reviewing the site’s written informed consent procedures, consent forms, and training records for study staff.
- Observe the… Read full answer
Source: https://hireabo.com/job/2_3_0/Clinical%20Research%20Associate%20%28CRA%29