Copilot for Clinical Research, IRB, and Patient-Facing Study Work
To Know
Where:
Online
Organizer:
CIT Technology Training Program
Presented By:
CIT Technology Training Program Staff
About this Class
Jump into a course specially designed for clinical research teams, IRB-related stakeholders, and staff who support protocol development, consent materials, and study documentation. Discover scenarios such as drafting protocol sections, simplifying patient-facing language, searching prior protocol content, organizing review notes, and creating clearer meeting minutes and action trackers. This is especially relevant because your NIH work already includes AI-enabled support for the IRB protocol lifecycle, simplified consent forms, historical protocol search, and multilingual needs.