Clinical Research Training for the Investigational Site Team

European Centre for Clinical Research Training (ECCRT)
15.09.2014 - 16.09.2014  Brussels, Belgium
Course Content
This is a two-day introductory course specifically designed for clinical site personnel such as study nurses and study coordinators. This course is a must for people desiring to keep up-to-date with the current regulations and guidelines on performing clinical trials. Highlights of this course include a number of interactive workshops on how to prepare for a clinical trial, how to manage an active trial and how to motivate patients.
Learning objectives, training objectives
Familiarize participants with clinical research regulations and guidelines. Provide hands-on information on how to manage a clinical trial on site, including: building the site team, managing and tracking the active study and meeting objectives, etc.
Target Audience
Study nurses, nurses, pharmacists, radiologists, ...
Typical postgraduate careers and job opportunities
Site Coodinator, Study Coordinator, Study Manager, Site Manager, Study Nurse
ISO 9001:2008/ Q-for
Local Organizer

Enquiries and Registration:

Ms. Sunita Kelecom
Clinical Research
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
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