Duration: 1 or 2 days
Description:
The role of the monitor is a very important one and there are a number of difficult issues which monitors may have to face. This course provides the following:
- more in depth information on the role of the monitor
- workshop sessions discussing issues
- basic project and site management theory
Who it is suitable for:
The course is most suitable for monitors with at least 6 months experience, either of on-site monitoring or of managing contract on-site monitors.
Example content:
Review of clinical trial life cycle
Study management:
- Overview of planning tools
- Tracking
- Study start up
- Risk assessment and contingency planning
Problem solving theory
Optimising subject recruitment
Case studies - dealing with difficult issues at site
Audit and inspection
Fraud and misconduct
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