**Clinical Research Resources Office, BMC/BUMC**

Mary-Tara Roth, RN, MSN, MPH, Director, CRRO

[The Principal Investigator Role ](https://www.bumc.bu.edu/crro/training-education/pi-role-training/)webpage

This course occurs quarterly, usually in March, June, September, and November. It covers the responsibilities of PIs and FDA sponsor-investigators; explains the purpose of and criteria for IRB review; discusses monitoring, evaluation, and reporting of adverse events and unanticipated problems; identifies protocol adherence and safety plan strategies; and presents best consent and screening practices; and study documentation best practices to meet IRB requirements and support high quality research.

[Register no later than 8 am, June 6](https://redcap.bumc.bu.edu/surveys/?s=EY8W9XYWH4YA3JXP)

***Successful completion fulfills the PI GCP training requirement for 3 years.***