About this role
Job summary
This is an exciting opportunity for an experienced oncology or haematology nurse to join our team as a Research Nurse supporting our expanding ATIMP (Advanced Therapy Investigational Medicinal Products) portfolio. You will play a key role in delivering complex and innovative clinical trials, including cell and gene therapy studies, within the Clinical Trials Unit at the Bristol Haematology & Oncology Centre.
As a Research Nurse, you will coordinate and deliver a varied portfolio of academic and commercial clinical trials--spanning early-phase studies, advanced therapies, and standard investigational treatments. Working closely with the multidisciplinary team, you will ensure the safe delivery of trial interventions, high-quality data collection, clear communication, and strict adherence to study protocols. You will be part of a supportive, forward-thinking research environment that is continually evolving with the growth of advanced therapies, offering opportunities to develop specialist skills in this cutting-edge area of practice.
Main duties of the job
Coordinate and manage a portfolio of clinical trials in accordance with study protocols, ICH-GCP, research governance and Trust SOPs. Support the informed consent process and act as a key resource for patients, carers and colleagues regarding clinical trials. Deliver high-quality clinical care to trial participants, including assessments, monitoring side-effects, and accurate documentation. Administer trial-related treatments (including IV, oral and subcutaneous therapies such as chemotherapy), with training provided if required. Work closely with the multidisciplinary team, attending clinics, MDT meetings and ward rounds to ensure continuity of care. Perform venepuncture, sample preparation and handling in line with protocol requirements. Contribute to trial setup, protocol review and readiness activities. Provide support, leadership and training to colleagues and junior staff members involved in research. Deputise for Senior Research Nurses when required and contribute to the ongoing development of the Clinical Trials Unit.
About us
University Hospitals Bristol and Weston NHS Foundation Trust (UHBW) is one of the largest acute Trusts in the country, bringing together a combined workforce of over 13,000 staff and over 100 different clinical services across 10 different sites, serving a core population of more than 500,000 people across South West England. UHBW has been rated by the CQC as 'Good' overall and our staff are proud to deliver excellent care to the people of Bristol, Weston and beyond. As a forward- thinking multi-award winning Trust and a digital exemplar committed to improving patient care, our world-leading research and innovations are having a positive local and global impact. Our hospitals are spread across Bristol and Weston, join us and you can enjoy the very best of both worlds; city living within a stone's throw of the countryside or beside the seaside, both with easy access to all that the South West has to offer. UHBW is committed to safeguarding and promoting the welfare of children, young people and vulnerable adults. As an equal opportunities employer actively working towards a diverse workforce we aim to recruit and retain a workforce which represents the rich diversity of the local population at all levels and are committed to designing our services around the needs of individual patients and those around them. Anonymous information will be used from your application in order to ensure we're meeting our pledge.
Job description Job responsibilities Clinical Trial Coordination
Take daytoday responsibility for coordinating a portfolio of ATIMP clinical trials, ensuring compliance with all regulatory and governance standards including ICHGCP and Trust SOPs. Work collaboratively with investigators, clinicians and the wider Clinical Trials Unit to maintain accurate, uptodate trial information and ensure safe, efficient trial delivery. Patient Care & Clinical Responsibilities Assess and monitor patients throughout their trial participation, documenting outcomes, adverse events and relevant clinical observations. Administer investigational and standard treatments, including cytotoxic chemotherapy (training and competency support available). Act as a consistent point of contact for patients and carers, providing clear information and maintaining a patientcentred approach. Attend relevant clinics, MDTs and ward rounds to promote continuity of care and facilitate safe trial delivery. Trial Procedures & Data Quality Undertake venepuncture, sample handling, spinning, storage and transport according to study protocols. Ensure all data is collected accurately, promptly and in accordance with study requirements. Contribute to trial setup, including reviewing protocols, supporting ethics/R&D processes and preparing study documentation. Leadership, Training & Team Support Provide leadership, guidance and motivation to staff involved in research delivery. Support teaching programmes, training, and induction of colleagues across the Division. Deputise for Senior Research Nurses as required and support the strategic development of the Clinical Trials Unit. Participate in audits, quality improvement projects and divisional research initiatives. Additional Responsibilities Act as a link nurse (e.g. health & safety, manual handling) as required. Work flexibly across Bristol and Weston to support research throughout the cancer pathway. Attend studyrelated meetings and training locally, nationally or internationally. Maintain compliance with Trust policies on safeguarding, information governance, health and safety, and clinical governance.
Person Specification
Knowledge and Experience Essential
Recent and substantial experience in Oncology/Haematology Recent and substantial experience or knowledge of Clinical Research Knowledge of chemotherapy applied to patient toxicity management Proven clinical, and or organisational, and managerial Experience/ skills Experience working within a multidisciplinary team Ability to demonstrate clinical expertise and sound knowledge of clinical issues Demonstrate an understanding of the research/audit process
Skills and Abilities Essential
Demonstrate advanced nursing practice; with the ability to give IV medication including chemotherapy or willingness to become chemotherapy competent Able to undertake line care & venepuncture or willingness to learn Interested in and willingness to take part in On-going trial teaching programmes Possess good IT skills Ability to support the senior research nurse and CTU manager in strategic planning and day to day running of the Clinical Trials Unit Ability to work effectively as part of a team Evidence of organisational skills
Qualifications and Training Essential
Registered Nurse Level 1 Current NMC Registration Evidence of formal ongoing professional development Degree/diploma or willingness to undertake
Desirable
Formal teaching qualification ENB 237/N14/FLAP or equivalent
Aptitudes Essential
Personal insight and awareness with ability to recognise own limits Ability to work flexibly according to role need Enthusiasm for and desire to embed research within clinical practice Personal Focus on the 6 C's: Care, Compassion, Courage, Commitment, Competence and Communication
Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
Certificate of Sponsorship Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab).
From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab).
UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).
Employer details Employer name University Hospitals Bristol and Weston NHS Foundation Trust (UHBW)
Address BHOC
Clinical Trials Unit BS2 8ED
Bristol
BS28ED
Employer's website https://www.uhbw.nhs.uk/ (Opens in a new tab)