Druckansicht
 
 

Clinical Research Training for Clinical Trial Assistants

European Centre for Clinical Research Training (ECCRT)
Archiv
-
01.10.2014 - 02.10.2014  Brussels, Belgien
 
Kursinhalte
Clinical Trial Administrators have a crucial role to play in the clinical research process. They must adequately maintain all the project’s documentation, records and files and archive them according to stringent standards. In addition Clinical Trial Administrators also assist with periodical reviews of the clinical project records for accuracy and completeness in order to remain audit-ready.
Lernziele, Trainingsziele
Introduce the new CTA to drug development. Clarify the difference between medical care and clinical trials. Explain the why, the when and the how of essential study documents - processes of a clinical trial from start to end.
Zielpublikum
CTAs who are relatively new to the job - people working in other areas
Typische Postgraduate Berufsfelder und Berufschancen
CTA, Clinical Trial Administrator, Study Nurse, Nurse
Zertifizierung
ISO9001:2008/ Qfor
Lokaler Veranstalter
ECCRT
 

Anfragen und Anmeldung:

Frau Sunita Kelecom
 
Kategorien
Klinische Forschung
Dauer
2 Tage
Sprache
Englisch, Italian
Kosten
EUR 850,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
 
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