Clinical Research Training for Senior CRAs
European Centre for Clinical Research Training (ECCRT)
Archiv
03.11.2014 - 04.11.2014 Brussels, Belgien
03.12.2014 - 04.12.2014 Milan, Italien
30.03.2015 - 31.03.2015 Brussels, Belgien
29.04.2015 - 30.04.2015 Munich, Deutschland
18.06.2015 - 19.06.2015 Brussels, Belgien
Kursinhalte
In this 2-day course you will learn how to optimize your monitoring methods and skills, how to solve recruitment and site management issues and gain insights into protocol and CRF development, quality systems and audits. A detailed look at ICH-GCP and updates on the EU directives will also be given and a half-day session on communication skills will address issues such as how to reach a win-win situation with study site personnel and how to work within a team.
In this 2-day course you will learn how to optimize your monitoring methods and skills, how to solve recruitment and site management issues and gain insights into protocol and CRF development, quality systems and audits. A detailed look at ICH-GCP and updates on the EU directives will also be given and a half-day session on communication skills will address issues such as how to reach a win-win situation with study site personnel and how to work within a team.
Lernziele, Trainingsziele
To refine your knowledge of ICH-GCP, quality systems and audits. To provide an update on EU Clinical Trial Directives. Highlight important elements in the development of protocols and CRFs. To provide fundamentals of clinical report writing.
To refine your knowledge of ICH-GCP, quality systems and audits. To provide an update on EU Clinical Trial Directives. Highlight important elements in the development of protocols and CRFs. To provide fundamentals of clinical report writing.
Zielpublikum
Site Manager, Junior CRA, CRA, Clinical Research Associate, Study Coordinator, ...
Site Manager, Junior CRA, CRA, Clinical Research Associate, Study Coordinator, ...
Typische Postgraduate Berufsfelder und Berufschancen
Senior CRA, Advanced CRA, Project Manager, Team Leader, Clinical Team Leader, Line Manager CRAs, Manager CRAs
Senior CRA, Advanced CRA, Project Manager, Team Leader, Clinical Team Leader, Line Manager CRAs, Manager CRAs
Zertifizierung
ISO9001:2008/ Q-for
ISO9001:2008/ Q-for
Lokaler Veranstalter
ECCRT
ECCRT
Anfragen und Anmeldung:
Frau Sunita Kelecom
Klinische Forschung
Dauer
2 Tage
2 Tage
Sprache
Englisch, Italian
Englisch, Italian
Kosten
EUR 1.100,00
EUR 1.100,00
Veranstalter Kontakt
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
Marcel Broodthaers plein 8b5
1060 Brussels
Belgien
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