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Clinical Study Administrator

3 months ago

London, Greater London, United Kingdom ICON Full time
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in Oncology trials.


You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement.

This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.


The Oncology Senior 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 fulltime contract of employment with us and 100% embedded to one client
  • Officebased 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