Programme
Module 1
Our traineeship program starts with a training session called ‘Introduction to Clinical Research Practice’ provided by the Institute of Clinical Research (ICR).
Our training program is standardized throughout Europe in combination with local trainers who are able to give more specific insight into the local countries ethic committees, trial applications etc.
See more information on the Introduction to Clinical Trials Practice course.
Module 2
Our hands-on module focuses on acquiring the skills and developing the competencies of becoming a successful CRA. The components below are included during the traineeship.
We have traineeship programs which have a duration of three months or possibly as long as twelve months, depending on the pharmaceutical, CRO or medical device organisation where you will perform your traineeship. Each length of traineeship offers different conditions, however the final result which is reached by you is of high quality, irrespective of the length of the traineeship.
Final examination
There are two points of assessment in order to complete the CRA Traineeship. The first is the assessment which is done by your Clinical Team Manager, determining whether your level of work and competencies are at the level of a junior CRA at the end of your traineeship.
The second is a formal exam conducted by the Institute of Clinical Research, which will test your theoretical knowledge on performing clinical research, and also assess your practical experience in working in clinical research.
