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.
Past Events
THE EFFECTIVE CRA / CLINICAL TRIAL ADMINISTRATOR / COORDINATOR 2011 - 27-28 Jan 2011, The Rembrandt Hotel, London, United Kingdom (10867)
Important
Please, check "THE EFFECTIVE CRA / CLINICAL TRIAL ADMINISTRATOR / COORDINATOR" official website for possible changes, before making any traveling arrangements
