As the Principal Investigator of a research study, you are responsible to ensure
the safety and welfare of all human research participants enrolled in clinical research
studies at your site. A guidebook has been developed by Independent IRB, Inc. to assist you
in all phases of this process.
Please use this Investigator’s Guidebook as a tool when conducting research at your
research site. In addition, please make sure that your sub-investigators, study
coordinators, and regulatory compliance specialist become familiar with the guidelines
and requirements outlined in the guidebook as well as with any local, state, and
federal regulations.