Please join us virtually for our monthly IRB Brown Bag Session featuring Priya R. Tripathi, Assistant Director, Center for Education and Career Development (CECD), Northwestern University Clinical and Translational Sciences (NUCATS) Institute.
Based on the NUCATS CRC Basic Training curriculum, this presentation will introduce the core responsibilities of a clinical research coordinator, with an emphasis on participant protection, regulatory compliance, and day-to-day study management.
By the end of this presentation, participants will be able to:
1. Describe the role and responsibilities of a Clinical Research Coordinator (CRC) throughout the clinical research lifecycle, including study start-up, participant recruitment, study conduct, and closeout.
2. Identify key ethical and regulatory requirements for conducting clinical research, including informed consent, Institutional Review Board (IRB) oversight, Good Clinical Practice (GCP), HIPAA, and participant safety reporting.
3. Recognize essential clinical research coordination activities and documentation practices, including maintaining regulatory files, managing study visits and procedures, documenting adverse events, and preparing for monitoring and audits.
Register and submit your questions. We hope to see you there!
Cost: None
IRB Training
(312) 503-7653
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