Senior Research Nurse

Queen Victoria Hospital NHS Foundation Trust; East Grinstead; Vor Ort; GBP 40.000 - 48.000; Teilzeit

Zusammenfassung

Queen Victoria Hospital NHS Foundation Trust in East Grinstead seeks a part-time Clinical Research Nurse (30 hours/week) to join the Research and Innovation team. The role covers a range of studies from questionnaire projects to full CTIMPs and device trials, requiring excellent organisation, attention to detail and extensive clinical research experience.

You will coordinate participant care, consent processes, study assessments and data management while working with multidisciplinary teams to

Qualifikationen

• Registered nurse with NMC registration and ongoing CPD.
• Experience delivering clinical research including CTIMPs and device trials.
• Experience with cancer patient care and ophthalmic care is desirable.
• Proficiency with trial management systems (e.g., EDGE) and MS Office.

Aufgaben

• Coordinate the research-related care of participants across a portfolio of studies.
• Identify eligible participants through clinics and referrals.
• Provide study information and obtain informed consent where trained.
• Coordinate protocol-required assessments, investigations and follow-up.
• Maintain source documentation, case report forms and local research databases.
• Support monitoring visits, audits and inspections and ensure safety reporting.

Kenntnisse

Phlebotomy

ECG

Organisation

Interpersonal skills

Communication

Prioritisation

Ausbildung

NMC registration

CPD evidence

Jobbeschreibung

We are looking for an experienced Clinical Research Nurse - Part-time (30 hours per week)to join the Research and Innovation team at Queen Victoria Hospital.

We undertake work across a range of specialties, which means plenty of variety in the role - from questionnaire studies right up to full scale clinical drug/device trials. You'll need good organisational skills, high attention to detail, and considerable experience working in clinical research.

This is an excellent opportunity for a motivated research nurse or practitioner who can work independently while contributing actively to a supportive multidisciplinary research team.

Main duties of the job

The postholder will coordinate a portfolio of clinical research studies across the Trust's specialist services. They will identify and recruit eligible participants, support informed consent, coordinate research-related assessments and follow-up, and maintain accurate study documentation and data.

Working closely with principal investigators, clinical teams, support departments, sponsors and research networks, the postholder will help ensure that studies are set up and delivered safely, efficiently and in accordance with the protocol, Good Clinical Practice and applicable research governance requirements.

About us

Rated GOOD overall with outstanding care by the CQC. A specialist NHS hospital providing life-changing reconstructive surgery, burns care and rehabilitation services across the South of England and beyond.

We specialise in conditions of the eyes (corneoplastics), hands, head and neck cancer and skin cancer, reconstructive breast surgery, maxillofacial surgery and prosthetics, providing regional and national services in these areas of clinical expertise. Our world-leading clinical teams also treat more common conditions of the eyes, hands, skin, and teeth for the people of East Grinstead and the surrounding areas. In addition, QVH provides a minor injuries unit, expert therapies, a sleep service, and a growing portfolio of community-based services. Patients consistently rate QVH amongst the top hospitals in the country for quality of care.

Our success is underpinned by the skills and enthusiasm of our staff and a strong culture of partnership. We are fully committed to training and development of the workforce with support for continuing education and learning.

Job responsibilities

The postholder will:

• Coordinate the research-related care of participants enrolled in a designated portfolio of studies.
• Identify potentially eligible participants through clinics, operating lists, clinical referrals.
• Provide clear study information to patients, families and carers and undertake informed consent where trained, delegated and competent to do so.
• Coordinate protocol-required assessments, investigations, sample collection, treatment and follow-up.
• Collect, process, store and dispatch biological samples according to study protocols.
• Monitor participants for adverse events and ensure that safety information is documented, escalated and reported within required timelines.
• Maintain accurate source documentation, case report forms, electronic study systems and local research databases.
• Maintain inspection-ready study documentation and support monitoring visits, audits and inspections.
• Lead study feasibility, set-up and initiation, including liaison with principal investigators, sponsors and supporting departments.
• Monitor recruitment performance, identify barriers and contribute to actions that improve patient access and study delivery.
• Promote research awareness among clinical teams.
• Deliver studies to a consistently high standard in accordance with the approved protocol, ICH Good Clinical Practice, applicable UK Clinical Trials Regulations, the UK Policy Framework

Person Specification

Skills

• Competency in phlebotomy, ECG and other relevant clinical activities

Qualifications

• NMC registration
• Evidence of continuing professional development

Experience

• Experience of delivering research studies including CTIMPs and device trials
• Experience in new study feasibility and set-up
• Experience of dealing with patients and families in distress
• Experience of working with different study databases and clinical research management system (eg. EDGE)
• Experience of using MS office package (Excel, PowerPoint, Word)
• Experience of the care of cancer patients
• Experience in ophthalmic care
• Experience in plastic surgery specialty

Knowledge

• Knowledge of the clinical research life-cycle; from EOI, feasibility, and set-up to coordination and closure--including securing all regulatory approvals prior to recruitment initiation

Qualifications

• Knowledge of ICH-GCP, Clinical Trial Regulation 2004 and UK Policy Framework

Skills

• Organisation, problem solving and management skills
• Interpersonal skills and able to communicate complex information at all level
• Ability to analyse complicated information from trial protocol
• Sound prioritising skills and ability to manage own workload

Disclosure and Barring Service Check

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.

£39,959 to £48,117 a yearper annum pro rata