Clinical Study Administrator - Luton

Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and also graduates with a relevant educational background and solid understanding of clinical research.

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.

You will be collecting, assisting in preparation, reviewing and tracking of documents for the clinical trial application process. You’ll contribute to the production and maintenance of study documents, and be template and version compliant.

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