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Would you like to join our CTU?

medical statistician

Grade 7: £33,309 - £40,927 p.a

Closing date: Monday 18th July, 12 noon

Based in the UKCRC Fully Registered Clinical Trials Unit, co-located within the Centre for Statistics in Medicine in its host department of the Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, Windmill Road, Oxford, OX3 7LD.
We are seeking to recruit a Medical Statistician to join one of the larger academic Clinical Trials Units in the UK, the Oxford Clinical Trials Research Unit (OCTRU) This is an exciting opportunity to contribute to the design, undertaking, analysis and presentation of results of funded non-commercial clinical trials across all phases of trials and in multiple areas of medicine including surgery, rheumatology, trauma, orthopaedics and oncology.
As Medical Statistician you will provide expert input on the statistical aspects of the design and set-up of clinical research projects, working within a multidisciplinary team. You will provide advice on data collection, case report form (CRF) development, data validation, data cleaning and data management. You will produce statistical programs for analysis of study data, including generating, validating, and monitoring randomisation schedules and performing interim and final analyses. You will also contribute to publications for peer review.
For further details, please click here  

clinical trials assistant

Grade 4: £22,847 - £26,341 p.a

Closing date: Friday 1st July, 12 noon

We have an exciting opportunity for a Clinical Trial Assistant to join the Surgical Intervention Trials Unit (SITU) within Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS) based at the Botnar Research Centre, Oxford. As a Clinical Trials Assistant within SITU, you will be assisting the trial managers of the group in the successful delivery of research projects.

As a Clinical Trial Assistant, you will provide administration and data support on various projects on the SITU portfolio , under the guidance of the trial management team. You will also deal with routine trial queries, passing non-routine and clinical queries on to the appropriate staff/professionals and ensure queries are resolved within an appropriate time period. You will co-ordinate the timely collection of study data from collaborating hospital, carry out data entry, and general office duties such as photocopying, filing, faxing, dealing with mail and any other comparable tasks as required.

For further details, please click here