Surrey and Borders Partnership NHS Foundation Trust is looking for someone who is self-motivated, flexible and able to adapt to hanging demands, able to organise their own workload and prioritise work, able to remain calm and professional under pressure and able to respect confidentiality guidelines.
The primary role of the research nurse, within the Research Team at Surrey and Borders Partnership NHS Foundation Trust, is to support a portfolio of mental health and dementia clinical trials. You will be responsible for assessing and monitoring research participants, liaising with study partners, recruitment of trial participants, collecting and processing biological samples and participant data as per the trial protocol.
It is essential that the post holder has experience in clinical skills such as phlebotomy, cannulation and medication administration (Oral, Subcutaneous, Intramuscular and Intravenous).
Main duties of the job
* Deliver safe, high-quality clinical care to research participants within clinical trials.
* Support the identification, recruitment, and monitoring of participants in line with study protocols.
* Ensure accurate data collection, documentation, and reporting in compliance with regulatory standards.
* Administer clinical trial interventions and perform clinical assessments competently.
* Work collaboratively within a multidisciplinary team while managing a defined caseload.
* Maintain effective communication with participants, clinical teams, and research stakeholders.
* Contribute to the development, delivery, and governance of clinical research within the service.
* Maintain professional competence through ongoing education and adherence to training requirements.
Job responsibilities
* Collect and process laboratory samples (e.g. blood and urine), including use of centrifuge equipment.
* Assess and monitor participants, including recording vital signs, ECGs, and adverse events.
* Safely administer clinical trial medications via oral, subcutaneous, intramuscular, and intravenous routes.
* Conduct study visits across multiple settings, including clinical sites and community locations.
* Work autonomously to manage a caseload of research participants within a multidisciplinary team.
* Assess eligibility and monitor participants throughout their involvement in clinical trials.
* Contribute to continuous improvement within the clinical research environment.
* Maintain up-to-date knowledge of clinical and research practices to enhance participant care.
* Identify, approach, and screen potential research participants.
* Ensure informed consent is obtained and participants fully understand study involvement.
* Conduct study visits and procedures in accordance with study protocols.
* Accurately collect, record, and manage study data within required timelines.
* Record, elevate, and report adverse events in line with study protocols and regulatory requirements.
* Adhere to ICH-GCP, research governance frameworks, and UK Clinical Trial Regulations.
* Support the setup, coordination, and management of clinical trials and trial documentation.
* Maintain clear, professional, and sensitive communication with participants, carers, and staff.
* Liaise with Principal Investigators, sponsors, and R&D teams to ensure smooth study delivery.
* Collaborate with clinical teams to promote research participation within the Trust.
* Build and maintain effective working relationships across departments and external organisations.
* Work closely within the research team to ensure coordinated and efficient practice.
* Take responsibility for maintaining and developing clinical and research knowledge and skills.
* Complete all mandatory training and comply with professional and regulatory standards.
* Support and supervise colleagues in clinical procedures where appropriate.
* Educate participants and carers on research processes and study requirements.
Experience
* NMC Registered Nurse (RGN/RMN)
* 2 years post qualification nursing experience
* Competent and signed off in medication administration (Oral, Subcutaneous, Intramuscular and Intravenous)
* Competent and trained in phlebotomy and cannulation
* Holds a valid full UK driving license
* Experience working in a clinical trial as a Research Nurse
* Experience working with mental health and dementia patients
* ICH‑GCP training certificate or prepared to work towards achieving this
* Access to own vehicle
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.
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