| Starts: | Monday February 01, 2010 at 9:00am |
|---|---|
| Ends: | Tuesday February 02, 2010 at 5:00pm |
| Event Type: | Training/Seminar |
| Region: | Antwerp Area, Belgium |
| Location: |
European Centre for Clinical Research Training Keizer Karellaan 576 Sint Agatha Berchem, REGION BRüSSEL-HAUPTSTADT 1082 BE |
| Price: | 1000 EUR (VAT excl) |
| Website: | http://www.eccrt.com |
| Industry: | pharmaceuticals |
| Keywords: | Clinical Research Associate, Gcp, Training, Clinical Research, Professional, Brussels, Clinical Trials, Audits |
| Intended For: | Clinical Research Associate, CRA, Regulatory, Senior |
| Organization: | ECCRT |
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.
This 2-day course has been specifically designed for people with at least 2 years' experience as a Clinical Research Associate (CRA) and who want to set new goals and objectives in their career.