Job overview
This is an exciting opportunity for an experienced oncology or haematology nurse who is either already involved in clinical research or highly motivated to develop a research career. You will join our Clinical Trials Unit at the Bristol Haematology & Oncology Centre, playing a key role in coordinating and delivering a varied portfolio of clinical trials, including early‑phase studies.
Working closely with the multidisciplinary team, you will help ensure patient safety, high‑quality data collection, excellent communication, and strict adherence to study protocols—all within a supportive and forward‑thinking research environment.
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.
Clinical Trial Coordination
* Take day‑to‑day responsibility for coordinating a portfolio of clinical trials, ensuring compliance with all regulatory and governance standards including ICH‑GCP and Trust SOPs.
* Work collaboratively with investigators, clinicians and the wider Clinical Trials Unit to maintain accurate, up‑to‑date 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 patient‑centred 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 study‑related meetings and training locally, nationally or internationally.
* Maintain compliance with Trust policies on safeguarding, information governance, health and safety, and clinical governance.
Knowledge and Experience
* 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
* 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
* Registered Nurse Level 1.
* Current NMC Registration.
* Evidence of formal ongoing professional development.
* Degree/diploma or willingness to undertake.
* Formal teaching qualification ENB 237/N14/FLAP or equivalent.
* 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.
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