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Job summary

Main area
Surgery
Grade
Band 5
Contract
Permanent
Hours
Full time - 37.5 hours per week
Job ref
176-C-7403511-A
Employer
North West Anglia NHS Foundation Trust
Employer type
NHS
Site
Hinchingbrooke Hospital
Town
Huntingdon
Salary
£31,049 - £37,796 per annum
Salary period
Yearly
Closing
12/10/2025 23:59

Employer heading

North West Anglia NHS Foundation Trust logo

Research Nurse - Huntingdon

Band 5

Job overview

***Please note we are only able to accept applications from those with a live UK NMC registration as we are unable to support OSCE at this time***

Are you an experienced and innovative NMC Registered Nurse? Would you like to apply your knowledge and skills to a research setting?

This is a unique opportunity for an enthusiastic NMC Registered Nurse to join our Research team and help us deliver high-quality research.

Our team consists of both clinical and non-clinical staff, local clinicians, and research groups. As workload dictates, cross clinical divisions will be required.

This is a permanent role based at Hinchingbrooke Hospital.  You may be required to work across sites as required.

You will demonstrate excellent communication and interpersonal skills, along with attention to detail.

Your research skills and knowledge acquired through proven CPD will be valuable to our research team. Training will be provided; however, you will be familiar with GCP.

You will collaborate with local R&D members to assess capacity and capability for research studies, working with members of the research teams to inform potential participants of relevant projects.

We are committed to ensuring that you achieve your full potential and have a rewarding career in research.

 

 

Main duties of the job

You will be working effectively within our clinical research team across the Trust supporting the staff, manage caseload of patients.

You will maintain effective communication with patients, carers and professionals to ensure service delivery. You will provide research information to patients and their relatives, and act as a resource and support to them, explaining practical aspects of clinical research.

Patients’ consent in research is very important. Therefore, you facilitate the informed consent process, in compliance with Good Clinical Practice (GCP), ensuring that the patient and relatives fully understand the nature of the research.

A main responsibility of your role will be ensuring that the study-specific investigations are undertaken as required by the research protocol, to ensure safety of study participants  safety to enter the study.

As part of your research duties, you will monitor treatment toxicity/side effects and ensure changes to treatment as required by the research protocol. You will arrange collection of blood and any other research samples required as part of the clinical research, and ensure safe and appropriate storage of specimens in conjunction with local clinical and nursing teams, phlebotomy and laboratory staff.

We are strongly encouraging you to contact Terri-Anne Baker, Research Team Leader or email  [email protected] for an informal chat about the role or to arrange a visit to learn more about what the role would involve.

Working for our organisation

We are committed to supporting colleagues through organisational change. Priority will be given to staff at risk within North West Anglia NHS Foundation Trust and Cambridgeshire & Peterborough Integrated Care Board.

Detailed job description and main responsibilities

The post holder will assist with participant identification and recruitment, obtaining informed consent from patients and will have responsibility for organising patient visits, collection and processing of patient samples, completion of case report forms and maintenance of study documentation according to Good Clinical Practice (ICH -GCP).

You will have experience of working within the Trust Divisions. Clinical research experience within the NHS is desirable but full training and mentoring will be provided.

The post holder will assist with participant identification and recruitment, obtaining informed consent from patients and will have responsibility for organising patient visits, collection and processing of patient samples, completion of case report forms and maintenance of study documentation according to Good Clinical Practice (ICH -GCP). 

Please see attached Job Description and Person Specification for further details.

Person specification

Education and Qualifications

Essential criteria
  • NMC registered Adult Nurse
  • Evidence of continuous personal and professional development and a clear vision of their academic pathway
Desirable criteria
  • Good Clinical (GCP) Practice Certification or working towards completion of this training.
  • Evidence of relevant post registration qualifications

Knowledge & Experience

Essential criteria
  • Minimum of 1-year Clinical experience in a healthcare setting
  • Articulates understanding of prioritising clinical issues
  • Explaining complex concepts to patients/participants
  • Experience of using MS Office and Excel spreadsheet
  • Experience working within the within the UEC, Medicine, or surgical speciality
Desirable criteria
  • Experience of working in clinical research, participant recruitment or research delivery in any healthcare setting.
  • Awareness of or willingness to undertake ICH Good Clinical Practice (GCP)
  • Collaborating with other agencies
  • Role of Ethics, HRA, R&D legislation, and the consent process in clinical research

Key Skills

Essential criteria
  • Experience of working effectively both independently and as part of a team
  • Excellent organisational skills, including the ability to prioritise a caseload and manage time effectively.
  • Effective communication skills with participants, carers and families
  • Effective communications skills, both written and oral with the ability to explain complex concepts to colleagues, participants, carers and relatives.
  • Demonstrates commitment to the principles of clinical governance and clinical supervision
  • Phlebotomy skills or willingness to undertake
Desirable criteria
  • Experience in managing data with meticulous attention to detail and accuracy in data collection skills.
  • Demonstrated skills in a range of disciplines
  • Presentation skills
  • Competent with database applications and data presentation

Employer certification / accreditation badges

NHS Pastoral Care Quality AwardApprenticeships logoNo smoking policyPositive about disabled peopleAge positiveDisability confident leaderInvestors in People: GoldMindful employer.  Being positive about mental health.Stonewall equality policy. Equality and justice for lesbians, gay men, bisexual and trans people.Step into healthDefence Employer Recognition Scheme (ERS) - GoldArmed Forces Covenant

Applicant requirements

You must have appropriate UK professional registration.

This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.

Application numbers

This vacancy may close earlier if it received a high number of applications and therefore we recommend that you complete and submit your application in good time to avoid disappointment.

Documents to download

Apply online now

Further details / informal visits contact

Name
Terri-Anne Baker
Job title
Research Team Leader
Email address
[email protected]
Telephone number
01733 677402
Additional information

Please contact Terri-Anne Baker or email [email protected] for an informal chat about the role or to arrange a visit to learn more about what the role would involve.

Available Monday-Friday for informal visits or calls.

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