Job summary
- Main area
- Research
- Grade
- NHS AfC: Band 6
- Contract
- Permanent
- Hours
- Full time - 37.5 hours per week
- Job ref
- 213-CORP-7911503
- Employer
- King's College Hospital NHS Foundation Trust
- Employer type
- NHS
- Site
- Denmark hill
- Town
- London
- Salary
- £47,951 - £56,863 pa, including HCAS
- Salary period
- Yearly
- Closing
- 21/04/2026 23:59
Employer heading
CRF Research Nurse
NHS AfC: Band 6
King’s College Hospital NHS Foundation Trust is one of the UK’s largest and busiest teaching Trusts with a turnover of c£1.8 billion, 1.5 million patient contacts a year and more than 15,000 staff based across 5 main sites in South East London. The Trust provides a full range of local hospital services across its different sites, and specialist services from King’s College Hospital (KCH) sites at Denmark Hill in Camberwell and at the Princess Royal University Hospital (PRUH) site in the London Borough of Bromley.
We encourage all our staff to have a healthy work/life balance. In doing so, you can apply for flexible working from the beginning of your employment. We offer a range of options which are designed to suit different circumstances and priorities in line with service requirements.
Job overview
Assess, plan, implement, and evaluate expert research nursing care and provide support to patients attending the Department who have been or have the potential to be recruited onto a CTIMP or ATIMP trial. The Research Nurse will play a key role in ensuring that any research undertaken within the department safeguards the well being of the patients and is conducted according to Good Clinical Practice (GCP) and the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006. In conjunction with the other members of the team, facilitate the production of good quality of research.
The research nurse will facilitate and aid in the recruitment of patients to ensure high quality clinical studies and trials that will require the nurse to work flexibly across the disciplines to ensure the successful working of the clinical research facility. They will also act as a patient advocate providing support and assistance as required and assist in the co-ordination and management of a portfolio of early phase translational clinical research.
The post holder will take responsibility for supervising the safe administration of experimental therapies, and for monitoring the expected and unexpected side effects of drugs and other treatment modalities used in these trials.
Main duties of the job
This role involves delivering high-quality clinical care to patients and volunteers participating in clinical trials (CTIMP and ATIMP), ensuring all procedures are carried out in line with study protocols, Trust policies, and regulatory standards such as ICH-GCP and MHRA guidelines.
The post holder is responsible for recruiting and following up participants, performing clinical procedures (e.g. venepuncture, drug administration, monitoring), and maintaining accurate clinical and research documentation. They act as a patient advocate, ensuring informed consent and supporting participants throughout their research journey.
In addition, the role includes administrative responsibilities such as coordinating resources, maintaining a safe clinical environment, supporting audits and regulatory processes, and contributing to service development.
The post holder also supports education and training by mentoring staff and students, promoting research awareness, and ensuring continuous professional development within the team.
Working for our organisation
The Trust provides a full range of local and specialist services across its five sites. The trust-wide strategy of Strong Roots, Global Reach is our Vision to be BOLD, Brilliant people, Outstanding care, Leaders in Research, Innovation and Education, Diversity, Equality and Inclusion at the heart of everything we do. By being person-centred, digitally-enabled, and focused on sustainability, we aim to take Team King’s to another level.
We are at a pivotal point in our history and we require individuals who are ready to join a highly professional team and make a real, lasting difference to our patients and our people.
King’s is committed to delivering Sustainable Healthcare for All via our Green Plan. In line with national Greener NHS ambitions, we have set net zero carbon targets of 2040 for our NHS Carbon Footprint and 2045 for our NHS Carbon Footprint Plus. Everyone’s contribution is required in order to meet the goals set out in our Green Plan and we encourage all staff to work responsibly, minimising their contributions to the Trust’s carbon emissions, waste and pollution wherever possible.
Detailed job description and main responsibilities
Clinical
Carry out planned care required by the clinical trials protocol for a group of volunteers without direct supervision
- Ensure the assessment, planning, implementation and evaluation of evidence based, individualised patient/volunteer care.
- Responsible for recruiting to, and following up, patients within studies. This includes both randomised clinical trials (CTIMP or ATIMP) and other high quality clinical studies. The role will involve working closely with multidisciplinary clinical teams
- Act as a patient advocate enabling patients to make informed choices concerning their involvement in the clinical trials (CTIMP or ATIMP) and ensuring advice and information is provided.
- Ensure there is sufficient skill mix of staff for patient safety during clinical trials and ensuring that they are carried out within the Trust and Centre's policies and clinical trial protocol.
- Assist in clinical trials including venepuncture and cannulation of volunteers when necessary ensuring that they are carried out within the Trust’s policies, research governance, Medicines for Human Use ( Clinical Trials Regulations ) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP) and Data Protection Act.
- Undertake clinical tasks such as phlebotomy, analysis of blood specimens, IMP preparation, drug administration and clinical observation etc.
- Preparing laboratory and ward areas for trials; procuring and labelling tubes and containers for biological samples, processing biological samples and ensuring samples are stored appropriately or despatched for storage.
- Ability to get trained in laminar flow maintenance with the help of senior Clinical Research Practitioners and Research Nurses.
Administration
- Plan, organise and deploy staff according to ability and workload in order to meet volunteer needs.
- Ensure that nursing practices comply with Trust policies and procedures
- Communicate effectively at all times and maintain a harmonious working environment.
- Maintain a safe environment in accordance with the Health and Safety at Work Act.
- Assist the Nurse Manager in managing incidents, accidents and complaints in accordance with Trust policies and procedures.
- Assist in ensuring the availability of resources for volunteer care
- Ensure equipment is in good working order, and report appropriately when defective
- Participate in audits, eg; those undertaken by the Medicines and Health Care Regulatory Authority (MHRA) nursing audits and clinical benchmarking exercises and suggest any change to improve standards
- Ensure the economical use of resources
Education and Training
- Assist in the education and support of health care professionals to enable them to care for clinical trial patients and recruit to clinical trials where appropriate.
- Maintain an up to date knowledge of research related topics particularly related to clinical trials.
- Attend local and national meetings as appropriate and as agreed with the local co-ordinating centre.
- Assess the needs of volunteers, relatives and carers and provide them with information as requested.
- Educate and counsel volunteers, family and those who volunteer for clinical trials before, during and after clinical studies and investigations.
Person specification
Education and Qualification
Essential criteria
- NMC Registration
- Level 1 Registered Nurse (RN1) or Mental Health Nurse (RN3)
- Good Clinical Practice Certificate
Desirable criteria
- Relevant specialist course
- Research Qualification
Knowledge and Experience
Essential criteria
- Cannulation and vene puncture skills (key requirement)
- Experience in Clinical Research
- Competency in medication administration including IV drugs (key requirement)
Desirable criteria
- SACT Knowledge / Experience (SACT Passport Holder)
Skills and Competencies
Essential criteria
- Organisation and management skills. Teaching
- Computer skills; with Excel Spread sheets, CRF and patient database systems, email and Microsoft office packages
- Ability to work effectively under effectively under pressure
Desirable criteria
- Skills in managing Haematological Disorders
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
Documents to download
Further details / informal visits contact
- Name
- Dani Nebres
- Job title
- CRF Lead Nurse
- Email address
- [email protected]
- Telephone number
- 0203 299 7139
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