Netherlands, Utrecht (Utrecht City Campus)

Clinical Research Monitoring

when 7 July 2014 - 25 July 2014
duration 3 weeks
credits 5 EC
fee EUR 1820

All main aspects of clinical research monitoring will be covered during this intensive course. The course is an important step-up for working as a CRA (clinical research associate). It will also help to gain knowledge and skills in other aspects of GCP and clinical development, and in data management and document design.

Course leader

Dr A. A. van Dooren

Target group

- Health care students (medical, pharmaceutical, nursing etc.)
- Health care professionals who are (going to be) involved in clinical (drug) trials
- Anyone interested in clinical trial job opportunities (CTA, CRA)

Course aim

- To get a thorough insicht in applicable laws, rules, regulations and guidelines of clinical trials.
- To be able to monitor the conduction of a clinical trial and to report quality-releated findings.
- To communicate as a CRA (clinical research associate).
- To understand and be able to apply the principles of clinical data management

Credits info

5 EC
Certificate of Attendance

Fee info

EUR 1820: • € 1820 - Course + course materials + housing
• € 1350 - Course + course materials
EUR 0:


Utrecht Summer School doesn't offer scholarships for this course.

Register for this course
on course website