This is an exciting opportunity for an experienced oncology or haematology nurse who is 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.
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.
* Coordinate and manage a portfolio of clinical trials in accordance with study protocols, ICH‑GCP, research governance and Trust SOPs.
* Contribute to trial setup, protocol review, readiness activities and support teaching programmes, training and induction of colleagues across the division.
* Administer trial‑related treatments (including IV, oral, subcutaneous therapies such as chemotherapy), with training provided if required.
* Perform venepuncture, sample preparation and handling in line with protocol requirements; undertake sampling, spinning, storage and transport according to study protocols.
* Support the informed consent process and act as a key resource for patients, carers and colleagues regarding clinical trials.
* Document adverse events, monitoring outcomes, accurate documentation and maintain data quality.
* Provide support, leadership and training to colleagues and junior staff members involved in research; deputise for Senior Research Nurses as required.
* Attend relevant clinics, MDT meetings, ward rounds and other study‑related meetings to promote continuity of care and facilitate safe trial delivery.
* Participate in audits, quality improvement projects and divisional research initiatives; maintain compliance with Trust policies on safeguarding, information governance, health and safety, and clinical governance.
* Work flexibly across Bristol and Weston to support research throughout the cancer pathway.
Patient Care & Clinical Responsibilities
* Assess and monitor patients throughout their trial participation, documenting outcomes and adverse events.
* 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.
We are an equal opportunities employer and are committed to diversity, ensuring a workforce that reflects the rich diversity of the local population. Anonymous information will be used from your application where necessary.
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