Investigators Working with New England IRB

New England IRB encourages investigators to adhere to the highest standards of human subject protection when conducting clinical studies. Towards that end, we have compiled a comprehensive Guidance for Investigators.which provides important information about study site submissions, informed consent, SAEs, and much more.

We have also created a training program for investigative site personnel. Please take a moment to review the training information and take the test at the end of the reading.

For electronic submissions of site submission forms, please contact us for access to our FastTrack™ Web Portal. Not all studies are managed through FastTrack™. Prior to requesting access, please ensure with the study sponsor  that the study in question is being managed through FastTrack™.

Please contact us via email or phone (617-243-3924) with any questions about study site submissions or investigator sponsored studies.