Full course description
Welcome to our introductory session on adverse events in clinical research, designed specifically for research coordinators who are new to the field and/or our institution. This presentation will equip you with essential knowledge and skills to effectively track and manage adverse events, ensuring participant safety and maintaining study integrity.
Learning Objectives
At the conclusion of this class, you will be able to:
- Importance of Tracking Adverse Events: Discover why meticulous tracking is vital for safeguarding participants, complying with regulations, and ensuring the success of clinical trials.
- Definitions and Types of Adverse Events: Gain clarity on key terms such as Adverse Events (AEs), Serious Adverse Events (SAEs), and Serious Unexpected Suspected Adverse Reactions (SUSARs).
- Process of Capturing Events: Learn the steps involved in observing, documenting, and reporting adverse events.
- Escalation and Reporting: Understand basic principles and timelines for escalating adverse events.
- Real-Life Examples and Stories: Engage with real-world scenarios and stories that highlight the impact of effective adverse event management.
Audience: Research coordinators, nurses, faculty, staff, and post-doctoral scholars working on clinical research projects at Stanford University.
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Session Date: Wednesday May 20th, 2026
Time: 9:00 - 11:00AM
Location: Virtual Meeting. This class will be held LIVE on the date above.
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Clinical Research Professional Competency Domain: Clinical Trials Operations (GCPs)
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