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This is a newly developed online modular course. The course consists of a serious of PowerPoint presentations, which can be watched at your own time. Each module consists of sub-modules which together will give specific information about the various steps of the development and running of a clinical trial. The contents of the sub-modules build on each other; therefore, consecutive listening is necessary. Short MCQs based on the content covered need to be completed to successfully complete each module. The themes covered within each module will be up-dated on an annual basis – if necessary.
Module 1: Cancer Clinical Trials: From development to opening
This module will give an overall context for and explanation of Cancer Clinical Trials and explains basic terminology.
Basics about Clinical Trials
Protocol Development
Feasibility Assessment
Ethics and Regulatory Submissions
Data Protection and the Irish Landscape
Module 2: Cancer Clinical Trials: Running a Cancer Clinical Trial
This module is focused on the processes and responsibilities in relation to running a Cancer Clinical Trial.
Investigator Responsibilities
Study Oversight and Risk Management
Data Management
Dissemination of Results