Clinical Research Associate (CRA) Training

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Download Course Summary Leaflet

This interactive and engaging course was developed by industry experts with a wealth of clinical trial experience. It goes through the whole clinical trial process and also includes aspects of Good Clinical Practice and Good Documentation Practice/Essential Documents.

It is aimed at those working within clinical research in roles such as Clinical Trial Associate/Admin who wish to progress to, or have recently become, a CRA/monitor and want to receive full training/certification.


Learning Objectives

      • To gain an in depth knowledge of clinical trials, including their start-up, guidance and regulations
      • To understand what a CRA role entails before, during and after a clinical trial
      • To become familiar with the roles within clinical research
      • To have a basic understanding of Good Clinical Practice
      • To understand and be able to implement Good Documentation Practices, essential documents and document control
      • To know how to perform effective monitoring visits


Course Support

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The course won't progress to the next module unless all ticks are blue.