Clinical Study Administrator - Luton
- London
- Clinical Trial Support
- ICON Strategic Solutions
TA Business Partner
- Icon Strategic Solutions
About the role
Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Senior Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and a solid understanding of clinical research.
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.
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
A better career. A better world. A better you.
Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more
Day in the life
Teaser label
Inside ICONContent type
BlogsPublish date
01/26/2023
Summary
The CRO market has seen an unmistakable uplift in demand for its services in recent years. The call for personalised medicine, pricing pressures, and increasing complexity in clinical trials are j
Teaser label
Inside ICONContent type
BlogsPublish date
10/03/2022
Summary
In traditional clinical trials, patients must attend regular check-ins at hospitals or clinics but fully remote decentralised clinical trials (DCTs) and hybrid trials limit this by replacing the in-pe
Teaser label
Inside ICONContent type
BlogsPublish date
05/22/2022
Summary
Having enjoyed steady growth over the last several years, it’s predicted that the global clinical trials market will hit a value of $65.2 billion by 2025, and around 58% of this can be attributed to r
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