Clinical Research Nurse


Company:	NHS Jobs
Salary:	£38,488 - £46,852
Hours:	Full-time
Location:	London, SE1 9RT
Job type:	Permanent
Posting date:	30 Jul 2026
Closing date:	13 Aug 2026

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Summary

Clinical research Work autonomously within professional practice guidelines to manage a caseload of Haematology trial patients, ensuring a duty of care and providing support to patients and their families. Identify patients suitable for entry into clinical trials by attending Haematology clinics, screening medical notes, reviewing consultant referrals, and participating in Multidisciplinary Team (MDT) meetings. Participate in the informed consent process acting as a resource and support to patients and their families, ensuring consent is appropriately obtained and documented. Coordinate the research patient pathway from screening through to trial closure Administer trial drugs (including investigational medicinal products and systemic anti-cancer therapies-SACT) safely to trial patients, monitor and report side effects as outlined in the protocol. Advise and train the local nursing team who administer trial drugs, be aware of and report any side effects as outlined in the protocol Maintain adequate patients records and ensure all relevant information is documented in the patients medical and nursing notes Keep up to date with current practices for cannulation, phlebotomy, care of patients with Central Venous Access lines and handling and administration for cytotoxic chemotherapy Act as a role model for excellence in haematology-based research Lead on a portfolio of trials and coordinate patient participation, paying particular attention to accurate data collection and transfer and version control of essential documentation. Liaise with the clinical team to organise and ensure that trial specific investigations are undertaken according to the protocol and obtain the results Liaise with trial pharmacy to co-ordinate the availability and dispensing of trial drugs if required Process blood samples according to the trial-specific lab manual and organise the storage and shipment of protocol specific samples Work in accordance with all regulatory requirements including: local Standard Operating Procedures (SOPs) Good Clinical Practice (GCP) European Directives Medicines for Human Use (Clinical Trials) Regulations Research Governance Framework for Health and Social Care Human Tissue Act Lead on stock control and ordering of consumables Please review job description document for full responsibilities.

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