Reasons to attend
This course will train you in the basic, yet crucial areas within clinical monitoring. All typical tasks of a Clinical Research Associate (CRA) will become clear to you, from selecting the investigators until study site close-out, with a great focus on the “monitoring practice” and an introduction on the impact of digitalization.
- Documents and materials related to this course are included
- Globally recognised certificates awarded after test completion
- This course has been granted PharmaTrain Recognition
2-Day Face-to-face: 09h00-17h00
Webinars: 4 sessions of 3 hours
5 July from 13h30 to 16h30
6 July from 9h30 to 12h30
7 July from 9h30 to 12h30
8 July from 9h30 to 12h30
Focussing on the different phases of the life cycle of a clinical trial, this introductory course is specifically designed for people who have between zero to twelve months’ monitoring experience. The course covers all operational activities of monitoring.
Dummy trial documents are used in the interactive workshops to share real-life operations.
It is, however, mandatory to have previously attended training on “Good Clinical Practice (GCP)”, as the aim of this course is to enable you as a CRA to implement the GCP requirements into your daily monitoring tasks.
Become an expert in GCP with our classroom training
or our eLearning course