Skip to main content
Please wait, loading

Job summary

Main area
clinical research
Grade
Band 6
Contract
Permanent
Hours
Full time - 37.5 hours per week
Job ref
287-CEF-411-26
Employer
Liverpool University Hospitals NHS Foundation Trust
Employer type
NHS
Site
Aintree University Hospital
Town
Liverpool
Salary
£39,959 - £48,117 per annum
Salary period
Yearly
Closing
30/10/2026 23:59

Employer heading

Liverpool University Hospitals NHS Foundation Trust logo

Research Nurse

Band 6

Job overview

The Liverpool University Hospitals NHS Foundation Trust has an exciting developmental opportunity for a band 6 clinical research nurse post in rheumatology/MSK.

The successful candidate will be responsible for the day-to-day running of research studies, including patient screening, recruitment, informed consent processes, and data management. The position requires excellent communication and interpersonal skills, as well as the ability to work independently and meet tight deadlines. 

The primary base for the post is Aintree University Hospital.

 

Main duties of the job

To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality
To be responsible for the day-to-day management of, patient recruitment to research studies
To work on a daily basis with minimal supervision as part of a research team
To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols.
To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the Research Governance Framework.
To ensure that all data is collected and managed effectively and accurately
To contribute to all aspects of the planning, conduct and reporting of all clinical trials within the research speciality
Knowledge of clinical research including issues on ethics, law, drug development and management in clinical issues
Partly responsible for submissions to research ethics committees
Maintaining overall standard of care for patients at all times
Educational and developmental role
Ability to give advice on the organisation and management of research in progress
Liaison with sponsor companies and multi-disciplinary research teams


Working for our organisation

NHS University Hospitals of Liverpool Group (UHL Group) was formed on 1 November 2024, born from a shared aim to improve the care we provide our communities.

We are one of the largest employers in region, with over 18,900 colleagues who are dedicated to caring for our communities - from birth and beyond.

For the 630,000 people across Merseyside, we are their local NHS. We provide general and emergency hospital care, alongside highly specialised regional services that extend to more than two million people in the North West.

We operate from five hospital sites: Aintree University Hospital is the single receiving site for adult major trauma patients in Cheshire and Merseyside, and hosts a number of regional services including an award-winning stroke facility. Broadgreen Hospital is home to several elective surgical, diagnostic and treatment services, together with specialist patient rehabilitation. Liverpool Heart and Chest Hospital provide specialist services in cardiothoracic surgery, cardiology and respiratory medicine, both in the hospital and out in the community. Liverpool Women’s Hospital specialises in the health of women and babies, delivering over 7,200 babies in the UK’s largest single site maternity hospital each year.  The Royal Liverpool University Hospital is the largest hospital in the country to provide inpatients with 100% single en-suite bedrooms and mainly focuses on complex planned care and specialist services.

Detailed job description and main responsibilities


To assist the clinicians in the assessment of patients/volunteers for eligibility for research and monitoring of their condition throughout their participation.
To provide ongoing advice and information to patients/volunteers with regard to their participation in clinical research in order to facilitate effective informed consent.
To assist the clinicians to report and record any adverse events as dictated by Trust and Departmental protocols.
To assist the clinicians with protocol development and ethical approval.
To assist in the analysis of data and preparation of reports for presentation and publication.
To co-ordinate and carry out patient visits in accordance with study protocols, including co-ordinating special tests in other departments, collection of data, coding, data entry and patient support
To carry out treatment procedures and treatment interventions according to predetermined protocols, including venepuncture, venous cannulation, administering of intra-venous drugs and vital sign recording
To report on a regular basis to the Senior Nurse of the R&D department for professional support and guidance.
To ensure that all clinical research activity is ICH GCP compliant and conducted in accordance with the agreed protocols
To maintain a high standard of patient care in line with Trust and R&D policies and protocols and in accordance with the Research Governance Framework
To ensure that all data is collected and managed accurately
To carry out the collection, processing and shipping of biological specimens according to protocol requirements and follow up appropriately on alert values
To be involved in the education of patients and their various aspects of their disease
To ensure that patient safety is paramount in all procedures that take place for trial purposes
To ensure clinical and research documentation and record keeping is completed accurately and efficiently in accordance with the EU Directive, ICH GCP Guidelines.
To work within the N.M.C Code Of Conduct and scope of professional conduct
To have sufficient computer skills for the handling and management of
computerised data
To keep up to date with relevant medical literature, developments in clinical research methodology, monitoring and local regulatory and ethical requirements
To attend research network meetings, attend courses, conferences and study days in order to remain up to date with all relevant aspects of clinical research
To participate in the education and development of staff/students, e.g. clinical supervision and ensure that all personnel are adequately informed about, and comply with all details of the trials.
To participate in the education and development of student nurses.
The post holder will be expected to work clinical shifts in a ward environment if necessary

Person specification

Qualifications

Essential criteria
  • RGN
  • Current NMC registration
  • Attendance of recent short courses and/or study days on research
Desirable criteria
  • 1st level degree or studying towards
  • Research Qualifications

Experience

Essential criteria
  • Demonstrable experience of patient education and counselling, e.g. providing lifestyle advice
  • Clinical experience/qualification in venepuncture, IV cannulation
  • Supervision of student nurses
  • Previous experience of co-ordinating clinical research studies
  • Experience of liaison with staff at all levels in Healthcare
Desirable criteria
  • Previous experience within the research speciality
  • Appraisal and interviewing skills

Knowledge

Essential criteria
  • Knowledge of the principles and practice of clinical research and/or clinical trials
  • Understanding of the role & responsibilities of a Clinical Research Nurse
  • Knowledge of ethical and quality standards applicable to clinical trials, including EU Directive on ICH GCP requirements
Desirable criteria
  • Knowledge of the Health Service, R&D, the pharmaceutical industry partnership and relevant information sciences

Skills

Essential criteria
  • Ability to use a personal computer, (computer literacy and proficiency in MS Office / EDCL)
  • Skills in administration and project management
  • Good communication, presentational, training and interpersonal skills
  • Ability to meet tight deadlines and cope in a highly demanding environment
  • Ability to work independently and prioritise / own workload and to communicate effectively with all members of the multi-disciplinary team
  • Excellent and effective verbal and written communication skills
Desirable criteria
  • Skills in handling and management of computerised data
  • Skills required to evaluate and assist in developing new protocols
  • Skills in the analysis and interpretation of data

other

Essential criteria
  • Possession of tact and sensitivity to the needs of both patients and colleagues, including a commitment to confidentiality
  • Meticulous attention to detail and a high standard of accuracy
  • Flexible approach to working hours

Employer certification / accreditation badges

Fair Employment Charter Status - Aspiring LevelNHS Pastoral Care Quality AwardTrust IDVeteran AwareApprenticeships logoNo smoking policyPositive about disabled peopleInvestors in PeopleArmed Forces Covenant Gold AwardMindful employer.  Being positive about mental health.Carer confident logo, the employers for carers confident schemeDisability confident committedStep into health

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 early if it receives a high number of applications. Please complete and submit your application in good time to avoid disappointment.

Documents to download

Apply online now

Further details / informal visits contact

Name
Ayren Mediana
Job title
Senior Research Nurse
Email address
[email protected]
Telephone number
0151 529 5889
Apply online nowAlert me to similar vacancies