Clinical Research Nurse in Lindley inLindley PUBLISHED MON 9 JUN 2025 Jump to job information section
Job description
We are looking for a patient focussed, motivated, passionate nursewith an interest in clinical research and good project management skills.
This is an exciting opportunity to join our established and experienced clinical research team at Calderdale & Huddersfield NHS Foundation Trust. Due to our success and reputation in clinical research, we have recently become a 'spoke site' for the NIHR Commercial Research Delivery Centre to improve access to commercial research trials and new treatment options for our patients.
The post holder will be expected to work flexibly across different clinical areas and specialties at both our hospital sites.
At CHFT we are keen to embed research in everyday care, enhancing patient experience and outcomes through research and innovation, across many specialties across a range of portfolios both commercial and non-commercial.
The successful candidate will support senior research nurses and other clinicians to deliver clinical research, once trained and competent leading studies independently. The role will involve working flexibly within the team yet have the ability and confidence to work independently when needed.
A comprehensive induction and training program will be provided, as well as ongoing mentorship support and buddy system. Previous research nursing experience is not required. We would encourage nurses with experience from a range of clinical backgrounds to apply.
The post holder will:
Be expected manage a broad clinical workload and assist with recruitment of patients into research studies and their ongoing follow up across a range of clinical specialties.
Have responsibility for identifying potential patients for trial entry, assist in the informed consent process and co-ordinate screening tests and appointments throughout the trial.
Be responsible for managing a caseload of patients, collecting accurate data, arranging tests, examinations and appointments according to specific research project protocols and local processes across a range of specialty areas.
Be visible in clinical areas working effectively both independently and as part of a team to offer clinical research options to patients and oversee their care and participation in research trials.
About us
See job description for full details. Due to limited word count, only a few points are mentioned below: Contribute to the set-up of research studies; assist in the feasibility process, liaising with support departments within the Trust, local investigators, trials units and R&D for local approval. Demonstrate enthusiasm and flexibility in supporting a variety of research studies, ranging from observational studies to Clinical Trials of Investigational Medicinal Products Assist in the selection and recruitment of participants in compliance with study inclusion / exclusion criteria Comply with the informed consent process as detailed in the study protocol and for studies which are not Clinical Trials of Investigational Medicinal Products (CTIMPS) take consent in line with study protocol, ICH-GCP and Trust SOPs.
For further information about the post please contact Georgina Turner on or Matthew Robinson on .
If you're interested in this role but you have questions or you're not yet ready to apply, then please book a quick call with us and we'd be happy to answer any questions you have and tell you more about the role.
Requirements
See the job description for full role requirements.
Benefits
Benefits are provided by the employer and will be confirmed during your application.
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