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Clinical Research Fellow Inflammatory Bowel Disease

Job in Southampton, Hampshire County, SO15, England, UK
Listing for: University Hospital Southampton NHS FT
Seasonal/Temporary position
Listed on 2026-08-24
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 42000 - 55000 GBP Yearly GBP 42000.00 55000.00 YEAR
Job Description & How to Apply Below

Job Overview

University Hospital Southampton NHS Foundation Trust is delighted to offer a fantastic opportunity to work with us in the Biomedical Research Unit.

Job Title: Clinical Research Fellow Inflammatory Bowel Disease

Start Date: September 2026

Contract Type: Fixed term

Duration: 12 months

Purpose for Fixed Term: Short term funding

This post is appointed on a fixed-term basis for the primary purpose of providing structured training and supervised clinical development. While the postholder will contribute to service delivery, the overarching purpose of the post is to provide defined educational opportunities, supervised clinical practice, and experience aligned to the relevant specialty training curriculum

Further details about the role can be found in the job description below.

Main duties of the job

As part of our team, you will work collaboratively with colleagues, helping to deliver excellent services and ensuring the highest standards of patient care. As part of the expansion of the Southampton Clinical Research programme, a new clinical research fellow post is available. 50% of your time will be spent on research service provision to Inflammatory Bowel Disease (IBD) and other studies at the SC  and UHS.

The remaining 50% of your time will be available to be spent supervised by a designated clinical academic with the intention of providing the time and support for an application to be made for a formal research training fellowship (eg MRC, Wellcome Trust or NIHR RTF) and registration for study towards a higher degree (usually PhD). The post will be appointed for 12 months in the first instance.

The position is available from 7th September 2026. It would suit a highly motivated individual who would like to gain experience of running research trials as well as developing their own studies.

Working for our organisation

As one of the largest acute teaching Trusts in England, we offer learning and development opportunities to help you achieve the career you aspire to. UHS is rated ‘Good’ by the CQC and in the latest national NHS Staff Survey, we were in the top 10 acute trusts for staff engagement and for staff recommending the hospital as a place to work or receive care.

We support flexible working and will consider requests taking into account the needs of the service. UHS employees are able to access a range of NHS discounts, are entitled to a minimum of 35 days paid holiday (pro rata), and we offer a generous pension scheme.

Southampton is an attractive place to live and work situated on the south coast, with an international airport and direct trains to London. The New Forest National Park and beaches of the Jurassic coast are also right on our doorstep. The city offers living costs 30% lower than London and 17 schools rated outstanding by Ofsted.

We believe that using technology wisely shows strong time management and commitment to innovation. However, personalising your recruitment application to highlight your unique skills and experiences is crucial. Relying too heavily on generic, AI-generated content instead of drawing from your own strengths and accomplishments may lead to your application being rejected if multiple candidates present identical or similar information.

Detailed

Job Description And Main Responsibilities

The successful candidate will be responsible for supporting the delivery of safe, effective, and patient-centred care while working collaboratively with colleagues across the organisation.

  • The primary role of this post is to assist the Directors and investigators in the running of clinical studies for patients in the CRF and Wessex Research Hubs including early phase clinical trials of vaccines, biological agents and other new drugs.
  • You will therefore be expected to engage as appropriate with all aspects of the development and conduct of studies, including the submission and maintenance of regulatory documents, the recruitment of subjects and providing medical cover.
  • You should work to ensure that all studies are conducted to Good Clinical Practice.
  • Working patterns are flexible depending on the study and visit requirements. Some out of hours working is required and contribution…
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