Clinical Trial Administrator
Location | Cheshire |
Discipline: | CRO & Vendor Services |
Job type: | Permanent |
Salary: | £Pounds |
Contact name: | Grace Ticehurst |
Contact email: | Grace.ticehurst@rbwconsulting.com |
Contact phone: | 01293 584300 |
Job ref: | 22228 |
Published: | over 2 years ago |
Expiry date: | 26 Jul 2023 11:59 |
Clinical Trial Administrator
Cheshire UK
12 month FTC
£30,000
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.
Accountabilities:
•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
Minimum Requirements
•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 grace.ticehurst@rbwconsulting.com
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