Clinical Research Fellow in Biomedical Ultrasound for Wound Therapy


Company:	University of Oxford, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences
Salary:	£38,831 - £52,656
Hours:	Part-time
Location:	Oxford, OX3 7LD
Working pattern:	On-site
Job type:	Contract
Posting date:	4 Aug 2026
Closing date:	18 Aug 2026

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Summary

The University of Oxford is a stimulating work environment, which enjoys an international reputation as a world-class centre of excellence. Our research plays a key role in tackling many global challenges, from reducing our carbon emissions to developing vaccines during a pandemic.

The Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS) is part of the Medical Sciences Division and is the largest European academic department in its field, running a globally competitive programme of research and teaching. Botnar Institute for Musculoskeletal Sciences enables and encourages research and education into the causes of musculoskeletal disease and their treatment. The Institute provides world-class facilities for scientists in the field of musculoskeletal research.

What We Offer

As an employer, we genuinely care about our employees’ wellbeing and this is reflected in the range of benefits that we offer including:

• An excellent contributory pension scheme

• 38 days annual leave

• A comprehensive range of childcare services

• Family leave schemes

• Cycle loan scheme

• Discounted bus travel and Season Ticket travel loans

• Membership to a variety of social and sports clubs

About the Role

In this role you will act as the Key Local Investigator on the study. In this crucial role you will be expected to communicate effectively with participants, patients, carers, the research team and other professionals as appropriate to ensure that the trial protocol and Standard Operating Procedures (SOP) are adhered to. You will provide support for Prof Fadi Issa including attending multidisciplinary meetings and clinics as appropriate, maintaining accurate participant’s records and ensuring all relevant information is documented in the medical notes and source data files. You will be responsible for the counselling and consent of potential patients in Study ensuring potential participants have received the appropriate oral and written information about the research project and confirming their suitability.

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