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IRB > Getting Started
Getting Started
A
Guide for Investigators and Research Staff
Who must be included on my protocol?
All key research personnel must be included on the research protocol. “Key
research personnel” include all persons who will have a significant
role in the design or conduct of the research, and includes at a minimum the
Principal Investigator, Co-Investigators and any other individuals who are
individually named on a grant or contract application, who are listed on
an FDA form 1572 (for the conduct of the research at UIC), who are named
as contact persons in the informed consent documents or recruitment materials
for research, or who provide supervision of the persons who are obtaining
informed consent to participate in research.
Additionally, any individuals (including student researchers and coordinators)
who are involved with the research by handling protected health information
or are using the research information or data set as part of their own research
should be included as research personnel on a protocol application.
If students or other individuals have minor roles in the research that are not
listed above, they are not required to be listed on the research protocol.
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