This two-day 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.
Focussing on the different phases of the life cycle of a clinical trial, this introductory two-day 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 a 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.