Clinical Research Training for Senior CRAs

European Centre for Clinical Research Training (ECCRT)
Archivo
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03.11.2014 - 04.11.2014  Brussels, Belgium
 
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03.12.2014 - 04.12.2014  Milan, Italy
 
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30.03.2015 - 31.03.2015  Brussels, Belgium
 
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29.04.2015 - 30.04.2015  Munich, Germany
 
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18.06.2015 - 19.06.2015  Brussels, Belgium
 
Contenido de curso
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.
Objetivos de formación
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.
Destinatario
Site Manager, Junior CRA, CRA, Clinical Research Associate, Study Coordinator, ...
Oportunidad de trabajos y los campos profesionales mas buscados por personas ya tituladas
Senior CRA, Advanced CRA, Project Manager, Team Leader, Clinical Team Leader, Line Manager CRAs, Manager CRAs
Certificación
ISO9001:2008/ Q-for
Organizador local
ECCRT
 

Información e inscripción:

Ms. Sunita Kelecom
 
Categorías
Investigación clínica
Duración
2 Días
Idioma
Inglés, Italian
Costos
EUR 1.100,00
Cantacto organizador
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
 
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