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Management Forum - A Cut Above the Rest
CPD Accreditation Advert
PHARMACEUTICAL
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THE EFFECTIVE CRA/
CLINICAL TRIAL
ADMINISTRATOR /
COORDINATOR - How
to be more proactive
in your role

Conference Date: 27-28 Jan 2010
Conference Ref: A1-4010
Fee: £1125 + VAT
Venue: The Rembrandt Hotel, London

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.

Click here to book your place on this important Annual Event