Clinical Research Training for Senior CRAs

European Centre for Clinical Research Training (ECCRT)
03.11.2014 - 04.11.2014  Brussels, Belgium
03.12.2014 - 04.12.2014  Milan, Italy
30.03.2015 - 31.03.2015  Brussels, Belgium
29.04.2015 - 30.04.2015  Munich, Germany
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.
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
ISO9001:2008/ Q-for
Organizador local

Información e inscripción:

Ms. Sunita Kelecom
Investigación clínica
2 Días
Inglés, Italian
EUR 1.100,00
Cantacto organizador
Marcel Broodthaers plein 8b5
1060 Brussels
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Ärzte der WeltCenter of ExcellenceÖsterreichische Gesellschaft für Public HealthCentro per la Formazione Permanente e l'Aggiornamento del Personale del Servizio SanitarioHelix - Forschung & Beratung WienÖsterreichische Akademie der ÄrzteHilfswerk AustriaAlumni Club Medizinische Universität Wien