Study Nurse Qualification
Intensive course 
Contents:
• Introduction to clinical trials
• Legal guidelines and regulations in clinical research (ICH/GCP)
• Responsibilities of investigators, study nurses and monitors
• Submissions, applications and registration
(Ethics Committee & authorities)
• Study Protocol and patient information
• CRF, source data and electronic documentation
• Study medication / laboratory
• Investigator Site File
• Adverse events (AE/SAE)
• Study coordination
• Coordinating and conducting clinical trials
• Monitoring visits: recruitment, qualification & initiation
Aim:
This intensive course specifically addresses practicing healthcare professionals. It provides you with a recognized qualification in Clinical Research and all the knowledge you require to work as a Study Nurse or Study Coordinator.
Dates:
30.08. - 03.09.2010
24./25./26.09. + 09./10.10.2010
08.11. - 12.11.2010
06.12. - 10.12.2010
Venue: PAREXEL-Akademie, Berlin
Cost: € 1.000,- + VAT
Download registration form (available in German)
Download flyer (available in German)
Download terms and conditions (available in German)