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 IIRB, 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.

Please click here to view Investigator’s Guidebook.