An error occurred in processing an image on this page.

Pharmaceutical Event: Essentials of Clinical Trial Monitoring (G8) |
Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds RSS Feed PharmiWeb Candidate Blog RSS Feed PharmiWeb Client Blog


Event Details


Essentials of Clinical Trial Monitoring (G8)

Essentials of Clinical Trial Monitoring (G8)

Add this event to your calendar: iCal   Google Calendar

Who should attend?

This course is for all those involved in clinical research monitoring. It covers a wide range of topics and is designed for those who have been in the role for only a few months as well as the experienced CRA.


This practical course defines the role of the clinical research monitor and explains the interaction with others in key roles as part of the clinical trial process as well as exploring the more complex aspects of clinical trial monitoring. Guidance will be given on best practices for selecting investigators, conducting monitoring visits and safety reporting. Delegates will explore strategies for dealing with common clinical trial management issues and how to adopt a preventative approach to handling monitoring issues. The course also summarises the essential documentation required during the clinical trial and gives an introduction to the key requirements of clinical trial project management. The course uses a blend of trainer input, exercises and delegate interaction.


Member 450 GBP, Non Member 550 GBP, Discounts for those working in the NHS or Academia


James Christianson

Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.