Clinical Research Nurse

Job title: Clinical Research Nurse

Salary: Band 6 £44,895 pa

Responsible to: Head of Research / Lead Clinical Research Nurse

Hours: 37.5 per week

Clinical accountability: Research Clinical Lead Contract Initially six months fixed term

Location CLH research clinics

Base: On site, with flexibility across services

Key relationships: Director of Research and Business Intelligence; Research Manager; Senior Research Facilitator; research nurses and clinicians; GP practices and PCNs; participants; NIHR/RRDN; sponsors and contract research organisations (CROs); community and tertiary care partners.

Who We Are

Central London Healthcare CiC (CLH) is a federation of 27General Practices and 4 Primary Care Networks (PCNS) in Westminster caring for more than 275,000 registered patients. We provide Community and Primary Care services to our residents, in addition to a wide range of staffing, management and administrative support to our member practices. By working closely with our PCNs and other key partners, including the Local Authority and community organisations, we help people to stay well and live healthier lives for longer.

We operate Federation-led services including Respiratory and Spirometry hubs; Community Cardiology; Community Dermatology; Community Diabetes service; Access E-hub and Enhanced Access and we support PCNs with managing their NWL single offer contract of services and the National Network DES contract, including ARRS roles.

We are proud to have a unique model of community-led care and support to tackle imbalances and inequality in the system called ‘The Octopus’ and takes us on a journey as part of the Westminster Integrated Neighborhood Team (INT)

We work collaboratively with other partners in the commercial sector including joint ventures; research and consultancy.

Our Approach

Our approach is to deliver exceptional assistance to our 27 General Practice members and to operate our NHS contracts in a manner that supports our Practices and their patients by providing services economically, locally, promptly and in a familiar environment.

Our employees work flexibly according to the needs of our customers, typically onsite at our practices, or hub sites including South Westminster Centre or at our office at Capital House near Edgeware Road tube station.

Our Purpose

Our purpose is to transform Health and Wellbeing in our communities.

Our Vision

Our Vision is to be the Healthcare Provider of choice, rooted in primary care.

Our Values

Compassionate: we listen respectfully, offer the opportunity for different viewpoints, and are kind to each other

Accountable: we work with integrity, taking accountability for our work to achieve the highest quality outcomes

Resilient: we listen and with this feedback, we constantly build and improve

Pioneering: we champion change, embrace creativity and promote innovation and new ways of thinking

Aspirational: we nurture and motivate so our people are enabled to reach their full potential

Role summary

The post holder is an autonomous registered nurse responsible for the safe coordination and delivery of an allocated portfolio of clinical trials and other research studies, including commercial and non-commercial studies. Working with Principal Investigators (PIs), research colleagues and partner services, they will oversee study readiness, recruit and care for participants, maintain high-quality records and act as a key site contact throughout delivery and close-out.

The post holder will work in accordance with approved protocols, applicable UK clinical trial legislation, the UK Policy Framework for Health and Social Care Research, Good Clinical Practice (GCP), NMC standards and CLH policies. Clinical procedures and delegated study tasks must remain within their training, competence, authority and appropriate clinical oversight. The role is primarily on site and involves flexible working across CLH research clinics, GP practices and partner locations.

Clinical research delivery and participant care

• Take day-to-day responsibility for an allocated study portfolio, prioritising safe participant care and timely delivery from site set-up and initiation to recruitment, follow-up and close-out.
• Identify and screen potential participants using authorised systems and approved methods; apply protocol eligibility criteria and confirm clinical eligibility with the PI or delegated investigator where required.
• Lead and undertake informed consent where trained, competent and documented on the delegation log; provide balanced information, allow time for questions and support voluntary decisions without pressure.
• Independently undertake protocol-led nursing assessments, clinical observations and procedures within competence, including venepuncture, ECG, spirometry, sample handling and shipment where required.
• Administer study medicines or vaccinations only under the applicable legal mechanism, approved protocol, local policy and documented delegation. Support investigational medicinal product (IMP) storage, accountability, reconciliation and returns where delegated and within competence, working with the clinical research pharmacist and PI.
• Identify, assess, document and escalation adverse events and serious adverse events in line with protocol timelines and delegated responsibilities; notify the PI and sponsor as required, and respond promptly to deterioration or urgent clinical concerns.
• Coordinate protocol visits, investigations and participant follow-up within study windows; support retention and address barriers to attendance while respecting the right to withdraw.
• Promote dignity, privacy, accessibility and reasonable adjustments; recognise and escalation safeguarding concerns through the appropriate pathway.

Study coordination and data quality

• Contribute to feasibility and site initiation; confirm that relevant training, delegation, equipment, clinical pathways, source documents and approvals are in place before study activities begin.
• Coordinate research clinics and participant pathways with coordinators and administrative staff, ensuring appointments, investigations and reimbursement processes support efficient study delivery.
• Maintain complete, accurate and timely source records and CRFs/eCRFs; resolve data queries and oversee the quality of records for allocated studies.
• Maintain accurate, inspection‑ready Investigator Site Files and other essential site documentation, including current training and delegation records and version‑controlled approved documents.
• Monitor recruitment, visit completion and study milestones; identify delivery risks early and agree practical actions with the PI, Research Manager and wider team.
• Act as a key site contact for sponsors, CROs and monitors; prepare for and participate in monitoring visits, respond to findings and close agreed actions within required timelines.
• Identify, document and escalation protocol deviations and data‑quality concerns; support investigation, corrective and preventive actions, and their follow‑up.

Governance quality and safety

• Work to GCP, applicable legislation, the UK Policy Framework, approved protocols, CLH standard operating procedures and information governance requirements.
• Maintain confidentiality and use SystmOne and other approved systems only for authorised purposes, following study approvals and data protection requirements.
• Ensure study activities are performed only by appropriately trained and delegated staff; raise gaps in training, delegation or operational readiness promptly.
• Maintain safe clinical environments and equipment, including infection prevention, required checks and prompt reporting of faults, incidents, near misses and complaints.
• Support audit and regulatory inspection readiness, provide accurate site records and complete agreed actions.

Leadership communication and professional development

• Plan and manage an autonomous workload, seeking clinical or managerial advice when a decision exceeds competence or delegated authority.
• Work collaboratively with PIs, GP practices, partner services and the wider research team; explain study requirements clearly to participants and colleagues.
• Support induction, supervision and development of junior research staff and coordinators, and promote awareness of appropriate research opportunities across CLH.
• Complete mandatory and study‑specific training, maintain professional registration and competence, and contribute to appraisal, service improvement and procedure review.
• Undertake other duties reasonably consistent with the scope and grade of the post.

The role may involve travel between CLH, practice and partner sites. This job description may be reviewed as the service develops following discussion with the post holder.

Qualifications and training

Essential

Registered Nurse (Adult) with current NMC registration. Current GCP training.

Desirable

Relevant post‑registration clinical or research qualification.

Experience

Essential

Substantial post‑registration clinical experience and direct participant‑facing research delivery. Experience of screening against protocols, informed consent, clinical assessments, AE/SAE escalation, source documentation and CRFs/eCRFs. Ability to manage an allocated research caseload and prioritise independently.

Desirable

Commercial or CTIMP trial delivery; primary care research; Phase II–IV trials; monitoring or audit; mentoring or supervision.

Knowledge

Essential

Sound understanding of GCP, UK research governance, ethical requirements, confidentiality, safeguarding, infection prevention and professional limits. Ability to identify and escalation deviations and safety concerns.

Desirable

IMP accountability and vaccine trial requirements; primary care systems and pathways.

Skills

Essential

Competent venepuncture and specimen handling. Clear, sensitive communication with participants and colleagues. Strong organisation, accurate record keeping and confident use of electronic health records and study data systems.

Desirable

SystmOne, ECG, spirometry, centrifugation, sample shipment and electronic data capture systems.

Personal attributes

Essential

Compassionate, accountable and reliable. Calm under pressure, adaptable and committed to participant safety, teamwork and continuous learning.

Desirable

Interest in research access and service improvement.

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