Navigating research ethics and regulatory requirements can be challenging, especially when multiple offices, committees, and compliance processes are involved. This session provides a practical guide to understanding key research oversight functions and knowing where to turn for guidance at each stage of the research lifecycle.

Attendees will learn when to engage resources such as the Institutional Review Board (IRB), Regulatory Affairs and Clinical Trials, and other offices and committees within the Institute. This presentation will highlight common scenarios, potential pitfalls, and strategies for obtaining timely assistance.

Whether you are new to research or an experienced investigator, this session will help you confidently identify the right contacts, ask the right questions, and ensure your research remains ethical and compliant.