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Education & Training
Key Research Personnel – Who Qualifies?
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 all Principal Investigators and Co-Investigators, and any 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/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. However, the Principal Investigator is responsible to ensure that these individuals receive both adequate training, including human subjects protection training, and oversight in accordance to the roles these individuals perform in the research.
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