This course gives a deeper insight in data management of clinical research projects. Focus will be on EDC (electronic data capturing), and designing CRFs (Case Report Forms). Theories will be applied direclty by the students in computer workshops where data management techniques will be practiced.This 1-week course is especially meant for junior CRAs who already have some experience in monitoring, or for those students who have followed the introductory course on clinical reserach and monitoring (during the weeks preceding this one). We will discuss and participate in practical workshops on data preparation and data management, on electronic data capturing, on CRF design and various other advanced topics. A must for CRAs!

Period
21-07-2014 - 25-07-2014 (1 weeks)

Target group
health care students (medical, pharmaceutical, nursing etc.)health care professionals who are (going to be) involved in clinical (drug) trialsanyone interested in clinical trial job opportunities and medical information management

Course aim
to get a thorough insight in applicable laws, rules, regulations and guidelines of clinical trialsto communicate as a CRA (clinical research associate)to understand and be able to apply the principles of clinical data preparation and management



Credits
0.0 ECTS credits

Course fee
EUR 795[Convert to USD] 795 - Course + course materials + housing 595 - Course + course materials

Course leader
Prof. Dr. A. A. van Dooren

Scholarships
-

Utrecht University
Address: PO BOX 80148
Postal code: 3508 TC
City: Utrecht
Country: Netherlands
Website: http://www.utrechtsummerschool.nl
E-mail: summerschool@uu.nl
Phone: 0031302534400