Clinical Trial Administrator
12 month FTC
A position has arisen for a Clinical Trial Administrator to join a specialist CRO in UK. This organisation stands out for their expertise in oncology. This is a really good opportunity to join a growing drug development company, where you will be providing key support to a range of interesting clinical trials. You will be joining a busy department that requires a focused individual with an eye for detail. This is initially a FTC for 12 months office based in Cheshire.
•Support the clinical trial activities with regard to time, cost and quality and in accordance with SOPs, ICH-GCP guidelines and relevant regulations
•Set up and maintain the documentation folders associated with product development and the Trial Master File (TMF) in compliance with ICH-GCP
•Ensure the TMF index is kept up to date
•Coordinate the collection of essential documents during site set-up
•Assist the Project Managers in the production of study reports and updates as required
•Degree or equivalent qualification in life sciences or nursing
•A good understanding of ICH-GCP and regulatory requirements
•Proven track record in working within clinical research in the pharmaceutical or CRO environment
•Experience in maintaining Trial Master Files/Investigator Site Files
•Excellent verbal and written communication and interpersonal skills
If you are interested in applying please contact Grace Ticehurst for a confidential chat on 01293 584300 or email firstname.lastname@example.org
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