The R&D Forum will list jobs that are relevant to the sector and are posted by non-commercial organisations.
Any organisation that is non-commercial and has a vacancy that is of relevance to the health and care research community in the UK
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Current Vacancies
| Clinical Trial Administrator |
| Location: Oxford |
| Organisation: Oncology Clinical Trials Office (OCTO), Dept Oncology, Oxford University |
| Type: Either Full or Part Time |
| Basis of Employment: Contract |
| Grade/Salary: Grade 5 – £31,459 to £36,616 per annum (pro-rata for part-time) |
| Closing Date: 21 July 2025 |
| Description:
Department of Oncology, OCTO, Level 2, Cancer & Haematology Department, Churchill Hospital, Headington, Oxford, OX3 7LE 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 clinical 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. Due to the location, you will be required to apply for and obtain an NHS Honorary Contract 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). The post is based in Oncology Clinical Trials Office (OCTO), Level 2, Cancer & Haematology Department, Churchill Hospital, Headington, Oxford, OX3 7LE, and is offered on a full-time, fixed-term contract for 2 years in the first instance. Requests for part time hours (minimum of 80% FTE worked over four days) will be considered. An early start date would be preferable for this role. 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). 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 in working on oncology clinical trials in a non-commercial setting would be advantageous. |
| How to apply:
Application Process 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. Only applications received before noon on 21st July 2025 can be considered. |
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