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Clinical Study Administrator

5 months ago


London, United Kingdom ICON plc Full time

The Clinical Study Administrator assists in the coordination and administration of the clinical study activities in the study start-up team, and within the Local Study Team, ensures the quality and consistency of study deliverables to time, cost and quality objectives. - Reporting into the Clinical Administration Manager, you’ll be involved in the coordination and administration of clinical studies from the start-up to execution and close-out. For this post, it is desirable that you have similar clinical trial experience within the Pharmaceutical Industry.

Also, you will need to translate or give the appropriate support with the translation of documents when required. Working closely with the Project Leader and CRA teams, you will be working on a number of clinical studies at any one time. You need to be comfortable working in a fast-paced environment.

Sciences degree/equivalent.
- Permanent full-time contract of employment with us and 100% embedded to one client
- Office-based in the Luton area (England): minimum 3 days per week and 2 days working from home
- Competitive salary depending on level of skills and experience plus company benefits