Identifying and monitoring adverse events (AEs) is critical to protecting research participants and ensuring quality data. Assessment of AEs and timely documentation is crucial to research participant safety and critical components of good clinical practice (GCP). Clinical Research Nurses (CRNs) are responsible for education, protection, and safety of participants enrolled in clinical trials; consequently, understanding AE assessment, documentation, recording, reporting, and mitigating are essential CRN responsibilities. This webinar will highlight best AE practices for CRNs including quality assessments of AEs, tips to avoid common audit finding, and navigating complex AE situations.  

Presented by:

Elizabeth Ness, MS, BSN, RN, CRN-BC
Director, Office of Compliance and Education
Center for Cancer Research, NCI

Shaunagh Browning DNP, RN, FNP-BC, CRN-BC
Senior Director, Office of Human Subject Protections
Georgetown University