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
Course Content
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.
Learning objectives, training objectives
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.
Target Audience
Site Manager, Junior CRA, CRA, Clinical Research Associate, Study Coordinator, ...
Typical postgraduate careers and job opportunities
Senior CRA, Advanced CRA, Project Manager, Team Leader, Clinical Team Leader, Line Manager CRAs, Manager CRAs
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Local Organizer

Enquiries and Registration:

Ms. Sunita Kelecom
Clinical Research
2 Days
English, Italian
EUR 1.100,00
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
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