Research Nurse

Dyddiad hysbysebu:	12 Rhagfyr 2025
Cyflog:	£31,049.00 i £37,796.00 bob blwyddyn
Gwybodaeth ychwanegol am y cyflog:	£31049.00 - £37796.00 a year
Oriau:	Llawn Amser
Dyddiad cau:	28 Rhagfyr 2025
Lleoliad:	Taunton, TA1 5DA
Cwmni:	NHS Jobs
Math o swydd:	Parhaol
Cyfeirnod swydd:	C9184-25-1923

Crynodeb

Department: Department of Clinical Research Base: Musgrove Park Hospital / Yeovil District Hospital Why this role matters Clinical research changes lives. As a Research Nurse/Practitioner at Somerset NHS Foundation Trust, you'll help bring cuttingedge studies to patients across Somerset--supporting trials sponsored by the NIHR and industry partners--so that evidence-based care reaches the bedside faster. You'll be a trusted point of contact for patients and families throughout their research journey, ensuring every study is delivered safely, ethically, and to the highest standards. About the Department Our Clinical Research Department provides research governance, management, delivery support, and advice across the Trust. We operate two closely connected functions--Research Governance and Research Delivery--working as one team with a clear vision: to support groundbreaking research with our partners to improve the health of our communities, and a mission to embed a culture of research excellence where all colleagues can contribute and develop as research specialists. Role overview You will coordinate, deliver, monitor, and record the care and progress of patients involved in research studies and clinical trials, working as an integral member of a multidisciplinary team. You'll recruit participants, obtain informed consent, and provide comprehensive support to patients and carers throughout their involvement. The post focuses on the safe conduct of NIHR portfolio and industry-funded research, collaborating closely with the Regional Research Delivery Network South West Peninsula (RRDN SWP) to meet local research delivery targets. This role is funded within the RRDN SWP network structure overseen nationally by the NIHR. You'll ensure all trial activities comply with UK/EU legislation, Trust policies, Good Clinical Practice (GCP), and regulatory requirements--protecting participants' rights, safety, dignity, and wellbeing at all times. Key responsibilities Participant engagement and care Provide clear, compassionate information to patients and carers about study protocols, procedures, treatments, and followup; obtain informed consent and act as a consistent point of contact for trial participants. Safeguard participant autonomy by ensuring sufficient information is provided during consent and that privacy and dignity are always respected Conduct study visits and assessments in strict accordance with protocol and Trust policy; interpret results to assess care needs and refer to other health professionals when appropriate. Study delivery and data quality Plan and organise study activities, ensuring protocol adherence and GCP compliance; maintain meticulous attention to detail across paper and electronic data capture (EDC) systems. Collect, verify, and enter data into Case Report Forms and study databases; answer data queries within agreed timescales and archive data per GCP requirements. Process, prepare, store, and dispatch biological samples safely; complete all related documentation accurately at specified time points Report Serious Adverse Events (SAEs) promptly; support required study documentation including protocols, amendments, advertisements, and approvals. Collaboration and communication Liaise with Principal Investigators, study sponsors, Clinical Research Associates/Monitors, trial managers across sites, and local clinical teams; present study updates at departmental or ward meetings as needed. Maintain effective crosscover with research colleagues to ensure continuity of trial delivery during leave or sickness Build strong relationships with the Clinical Trials Pharmacy, diagnostics services, GPs, and other practice staff to facilitate seamless research delivery. Governance, safety, and improvement Adhere to ICHGCP, Trust SOPs, policies, and Clinical Governance requirements; promote health, safety, and security by identifying risks, attending essential training, and following agreed procedures. Contribute to progress reports and updates to the Lead Research Nurse, Research Team Lead, Research Manager, and Assistant Managers throughout each project. Seek patient and carer feedback and support the embedding of research as part of routine clinical care across the Trust. Clinical skills (with training) Undertake phlebotomy; perform ECG, spirometry, and centrifuge use where required by protocols (training provided). Within scope of practice and competency, administer study medication or teach patients to selfadminister, monitoring for toxicity in line with protocol. Operational flexibility Work flexibly to meet study needs, with occasional activity outside normal hours to maintain protocol integrity. Travel across Trust locations and to offsite meetings or training as required. What you'll bring Registered Healthcare Professional with recent experience in General Medicine, Surgery, Mental Health, or Community Care; strong communication skills (verbal and written). Ability to evaluate research significance, apply evidence to practice, and follow protocols with high accuracy--balancing data integrity with sensitive, personcentred care. Confidence with data collection, electronic systems, and documentation; proactive approach to recruitment strategies and embedding research in routine care. Calm under pressure, an excellent listener, and a collaborative teamplayer who organises time effectively and multitasks with attention to detail. Willingness to undertake physical aspects of the role (e.g., phlebotomy, data entry) and to work across different Trust locations when needed. Training & development You'll receive a thorough induction and training in research methodology, design, audit, and GCP, with opportunities to expand diseasespecific knowledge and develop new clinical and research skills. You'll also help train and support colleagues involved in studies, contributing to a culture of continuous improvement and clinical governance. Governance, equality, and safeguarding We are committed to equality of opportunity for staff and service users. You'll work in line with our E&D policies, safeguarding responsibilities for children and vulnerable adults, and confidentiality standards under the Data Protection Act (2018) and Trust policies. You'll participate in clinical governance and infection prevention and control, promoting a safe environment for patients, colleagues, and visitors. What success looks like in this role Highquality, patientcentred research delivery that meets NIHR and sponsor timelines. Flawless documentation and data integrity, with timely resolution of queries and safe sample handling. Strong, collaborative relationships across clinical teams, pharmacy, diagnostics, investigators, sponsors, and the RRDN SWP. Positive feedback from participants and carers; measurable contribution to embedding research across the Trust. Practical details Contract type / hours / salary: 37.5 hours, permanent post, working days are Monday to Friday. Reports to: Research Team Lead. Responsible for: Research delivery within the Department of Clinical Research. How to apply If you're motivated by improving patient outcomes through research, we'd love to hear from you. Please submit your application via NHS Jobs, outlining how your skills and values align with this role. Shortlisted candidates will be invited to interview, where we'll explore your experience of patient centred research delivery, data accuracy, and collaborative working. A note from our team You'll join a welcoming, supportive department where curiosity and compassion drive everything we do. Whether it's guiding a patient through consent, processing samples to exacting standards, or collaborating with sponsors to keep studies on track, your work will make a real difference--today and for years to come.