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United Kingdom (UK) 🛡️ UK Work Eligibility 💼 College / University
University of Oxford - Clinical Trial Administrator
University of Oxford ✓ Verified Employer

Clinical Trial Administrator

Verified Base Compensation
£27,131 - £32,348 / year
£2,261 - £2,696 / mo Apply Now →
Official Specifications

Role Overview & Mandate

Executive Summary

About the role We have an exciting opportunity for a Clinical Trial Administrator (CTA) to join the Oncology Clinical...

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About the role
We have an exciting opportunity for a Clinical Trial Administrator (CTA) to join the Oncology Clinical Trials Office (OCTO), working in a team of trial management professionals, running clinical trials and studies across a varied portfolio of trials. The post holder will be responsible for a range of activities required in the day-to-day running of trials. CTAs will usually work on 1-3 trials, offering the opportunity to be involved in and learn about a wide range of clinical trial management activities.
OCTO is based in the Department of Oncology, University of Oxford. OCTO develops and runs academic clinical trials and studies to the highest standards and is proactive in improving clinical trial procedures. Our trials are concerned with the practical application of high-quality clinical research into innovative and effective cancer therapies, early detection and prevention strategies.
The post is based in Oncology Clinical Trials Office (OCTO), Level 2, Cancer & Haematology Department, Churchill Hospital, Headington, Oxford, OX3 7LE, and are offered on a fixed-term contract for 2 years in the first instance. Due to the location, you will be required to apply for and obtain an NHS Honorary Contract in order to carry out this role.
There will be the occasional need to travel to participating hospitals or national meetings (approximately twice a year, sometimes with the need for overnight stays).
About you
You will be educated to at least A-level in a biomedical or associated subject (or other relevant qualification) and have previous experience in a clinical research setting, with knowledge of Good Clinical Practice (GCP) and the role of UK clinical research bodies (e.g. HRA, MHRA, NIHR). You will have experience of managing and working with clinical research or patient data e.g. data entry, data coding, entry validation and reporting, with critical and intelligent attention to detail and high standards of accuracy. You will have effective communication and inter-personal skills, including written and spoken English, and sound clerical skills, including word processing. Experience of working on oncology clinical trials in a non-commercial setting would be advantageous.
Application process
If you would like to discuss this role please contact Sarah Pearson on sarah.pearson@oncology.ox.ac.uk
You will be required to upload a supporting statement (setting out how you meet the selection criteria), a curriculum vitae and the names and contact details of two referees as part of your online application.
The closing date for applications is 12.00 noon on Monday 17th April 2023.
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Compensation Analytics

Estimated Take-Home Pay

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Projected statutory deductions based on standard single-filer baseline tax regulations in the United Kingdom corridor.

Gross Annual Package £27,131 - £32,348
Est. Income Tax Band 20% Basic Rate Band
Statutory Insurance / FICA 8% Class 1 National Insurance (NI)
Estimated Monthly Net £1,809 - £2,103 / mo
Regional Economics

Cost of Living (Oxford, England)

Bureau Data
Est. Rent (1-Bed)
£1,100 - £1,750
Monthly Utilities
£140 - £210
Cost Index
112.5
Disposable Tier
Top 15% Rank
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Compliance Standards

Work Authorization Framework

Verified Status: UK Work Eligibility
Corridor: UK Employment Corridor
🛡️ Zero Fee: Direct corporate recruitment with zero placement charges.

Candidate Selection Pipeline

Direct Corridor Track
01
Direct Apply

Submit verified credentials & CV.

02
HR Screening

2-4 day credential verification.

03
Technical Panel

In-depth domain & team interview.

04
Official Offer

Corridor contract & relocation.

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