Clinical Research Fellow

Overview

The University of Leicester invites applications for a Clinical Research Fellow within the Division of Respiratory Sciences. This collaborative project between Respiratory Sciences and Genome Biology is funded by the Midlands Asthma and Allergy Research Association and focuses on investigating potential biomarkers of airway hyperresponsiveness in individuals with asthma. The position is based at Glenfield Hospital within the NIHR Leicester Biomedical Research Centre asthma service. The successful candidate will be supported in applying for a higher degree and will hold a fixed term contract until February 2029. Existing staff members may also be considered for this role on a seconded basis.

Who can apply

Applicants must possess an MB BS or equivalent, hold full GMC registration with a licence to practise, and have an MRCP (UK) or an equivalent qualification. Candidates are required to have completed at least two full years of Foundation training or equivalent alongside experience working in Respiratory Medicine. A demonstrable commitment to research through academic training, conference presentations, prizes, or publications is essential. Applicants must also understand the data-protection, governance, and ethical requirements of clinical research, and hold or be able to obtain Good Clinical Practice certification. Advantageous qualifications include experience managing asthma patients, familiarity with research or statistical methodology, knowledge of data-analysis tools, or background in asthma-related research.

What you get

The position offers an opportunity to conduct research within a multidisciplinary environment and receive support to apply for a higher degree. The employer provides a pension scheme, annual leave allowance, and opportunities for professional development and career progression within a collaborative setting.

Requirements

The fellow will be responsible for screening, recruiting, and sampling research participants before and after methacholine challenge. Responsibilities include processing and recording study data and samples, participating in laboratory studies utilizing omics methods, and collaborating with both clinical and non-clinical colleagues. Additional duties involve analyzing and presenting findings, preparing scientific manuscripts and reports, helping coordinate the study according to ethical and research governance standards, and supporting participant clinical care. The role may also involve contributing to relevant outpatient clinics, supervising junior colleagues, and presenting research at international and national meetings.

Key dates

The closing date for applications is 23 November 2026.