Audience: Trial Coordinators with at least 12 months experience.
This course is aimed at Trial Coordinators who are responsible for the set-up, coordination and management of an entire study for a Chief Investigator. This course is not designed for research staff who are involved in study set up for a Principal Investigator.
Please indicate the length of your Trial Coordinator experience in your application
Aims & Objectives: The masterclass is set up to refresh prior learning and to share best practices involved in the coordination of trials.
Course Summary: Through a facilitated discussion, attendees will discuss and explore various aspects of trial coordination from set up and designing study documentation, coordinating the study, source data verification and amendments through to understanding the impact of trial coordination at inspection. The Masterclass refreshes prior learning through the following modules: Delivering Quality though Oversight, Consent is more than just saying ‘Yes’, Amendments – can they make or break a study?, and When Research Goes Wrong. The Masterclass is set up to allow for sharing of best practice.