The Effective CRA/Clinical Trial Administrator/Coordinator
Thursday, January 27, 2011 - Friday, January 28, 2011
To be Announced
London, United Kingdom
http://www.management-forum.co.uk/pharmaceutical/eventid/1452
Event Type: Conference
This interactive course will provide you with the skills and knowledge to be a successful and effective CRA or member of Clinical Trial Support staff. It covers all the key aspects which CRAs and support staff are likely to be involved in as well as the most important interpersonal skills necessary to be an effective CRA
This will include:
- Planning and preparation for setting up clinical trials
- Understanding the responsibilities at both the study site and the sponsor site
- How to carry out the crucial study site visits including
- How to prepare for an audit and/or regulatory inspection
- Technological advances on collecting data - EDC
- On finishing the course you will then be up to date on the latest regulatory GCP requirements including the EU Clinical Trial Directive and Implementation texts, and the GCP Directive.
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