Research Nurse, Midwife or Allied Health Professional

University of Oxford; Oxford; On-site; GBP 30,000 - 40,000; Full time

Job summary

A prestigious university in the UK is seeking an experienced Research Nurse to join their Critical Care Research Group. The role involves recruitment and management of study participants in clinical research, focusing on post-ICU rehabilitation. Ideal candidates will have ICU experience and a relevant nursing qualification. The position is full-time and fixed-term until August 2027, requiring on-site work to ensure patient safety and compliance with research standards.

Qualifications

• Experience as a Research Nurse, Midwife or Allied Health Professional.
• Ability to work both collaboratively and independently.
• Knowledge of Good Clinical Practice and Research Governance.

Responsibilities

• Recruit study participants and conduct data collection.
• Administer Trial Master File and provide research training.
• Ensure study management adheres to ethical guidelines.

Skills

ICU experience

Clinical research delivery

Qualitative interviewing

Education

Relevant nursing or health-related qualification

Job description

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Research Nurse, Midwife or Allied Health Professional, Oxford

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Client:

University of Oxford

Location:

Oxford, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

5cd80f1f0c0b

Job Views:

10

Posted:

12.08.2025

Expiry Date:

26.09.2025

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Job Description:

Nuffield Department of Clinical Neurosciences (NDCN), Kadoorie Centre, John Radcliffe Hospital, Headington, Oxford, OX3 9DU This role is for an experienced Research Nurse, Midwife or Allied Health Professional with ICU experience and an interest in post-ICU rehabilitation. Directed by the Chief Investigator, Sarah Vollam and Co-investigators in the Critical Care Research Group based in the Kadoorie Centre , the post holder will be involved with all aspects of clinical research delivery for the PROgnosiS Prediction after Enhanced or CriTical care (PROSPECT) Study and our other BRC-funded research projects. This will include screening and recruitment of study participants, data collection and participant follow up, in addition to Trial Master File administration and research training. There will also be opportunities to develop academic skills, including research design, qualitative interviewing and analysis, paper writing, dissemination and Patient and Public Involvement. The post holder will be able to work both collaboratively and independently to ensure that patients are safe and comfortable throughout all clinical study processes; and to ensure the study is managed in accordance with ‘Good Clinical Practice’ and ‘Research Governance’. This role principally involves on site working as it requires face to face contact with potential research participants. The post is full time for a fixed term until 31st August 2027 in the first instance.