Clinical Research Nurse

EMS Healthcare; Chester; On-site; GBP 35,000 - 45,000; Full time

Job summary

A healthcare research organization is looking for a Clinical Research Nurse (CRN) to evaluate wound hypergranulation using advanced 3-D imaging. The role involves participant screening, data collection, and ensuring high standards of clinical care and protocol compliance. Applicants should be Registered Nurses with GCP knowledge and clinical experience in wound care. This position offers ample opportunity for autonomous work while ensuring excellent patient experiences and accurate documentation. Benefits include generous annual leave and health support.

Benefits

Bank holidays plus 25 days annual leave

Enhanced Maternity and Paternity Leave

Healthshield

Cycle to Work Scheme

Electric Car Scheme

Wellbeing support from qualified Mental Health First Aiders

Qualifications

• Registered Nurse (Adult or Child branch) with active NMC registration.
• Good Clinical Practice (GCP) / ICH GCP training (or willingness to complete prior to study start).
• Evidence of ongoing professional development.

Responsibilities

• Screen participants in accordance with inclusion and exclusion criteria.
• Monitor for, document, and report adverse events (AEs).
• Support monitoring visits, data verification, and audit readiness activities.

Skills

Excellent interpersonal and communication skills (verbal and written)

High attention to detail and accuracy in documentation

Strong clinical judgement with appropriate escalation skills

IT proficiency including digital imaging

Education

Registered Nurse with active NMC registration

Degree in a related subject area

Job description

The Clinical Research Nurse (CRN) will play a key role in the delivery of an observational study evaluating wound hypergranulation using advanced 3‑D photographic imaging and Investigator‑led assessments. Working across designated UK sites, you will be actively involved in participant screening and consent, detailed wound assessments and imaging, accurate data collection, and safety reporting. This role offers the chance to work autonomously while maintaining the highest standards of clinical care, protocol compliance, and Good Clinical Practice (GCP). You will ensure excellent participant experience, high‑quality documentation, and adherence to study protocol EHCI HG 04‑01 and EMS Healthcare procedures. Deadline: 9th January 2026.

Clinical & Research Activities

• Screen participants in accordance with inclusion and exclusion criteria.
• Support and/or lead the informed consent and assent process in line with ICH‑GCP.
• Perform wound examinations and assist Study Investigators with clinical assessments.
• Capture high-quality wound images using LifeViz® Mini 3‑D photography equipment (training provided).
• Prepare wound areas and calibration tools (15 cm ruler) to ensure standardised imagery.
• Upload imaging securely to the central server according to study procedures.
• Collect patient‑reported outcome measures (Wound‑QoL‑14, PROMIS Scales).
• Complete all electronic case report forms (eCRFs) accurately and within required timelines.
• Maintain meticulous source documentation and site files.

Participant Care & Safety

• Provide compassionate, patient‑centred care to adults, adolescents, and children.
• Handle wounds and dressings safely in line with clinical best practice.
• Monitor for, document, and report adverse events (AEs) and serious adverse events (SAEs) in accordance with protocol and regulatory timelines.
• Escalate clinical concerns to the Study Investigator, Clinical Regional Manager, or Sponsor as appropriate.

Quality, Governance & Compliance

• Work in accordance with ICH‑GCP, EMS Healthcare SOPs, and the approved study protocol.
• Maintain confidentiality and ensure data is handled securely and in line with GDPR.
• Support monitoring visits, data verification, and audit readiness activities.
• Contribute to continuous improvement and protocol compliance across participating sites.

Collaboration & Communication

• Work closely with Study Investigators, site clinical teams, EMS Clinical Operations, and external research partners.
• Liaise with the CRO, central imaging vendor, and project managers as required.
• Communicate clearly with participants, carers, and multidisciplinary colleagues.
• Attend required training, study meetings, and site initiation activities.

Qualifications

• Registered Nurse (Adult or Child branch) with active NMC registration.
• Good Clinical Practice (GCP) / ICH GCP training (or willingness to complete prior to study start).
• Evidence of ongoing professional development / continued CPD.

  Experience – Essential

  • Clinical experience in wound care, tissue viability, surgical wounds, leg ulcers, or related areas.
  • Clinical research experience (observational or interventional).
  • Significant post‑registration clinical experience.
  • Competence in clinical assessment, communication, and documentation.
  • A good understanding of clinical research.

  Experience – Desirable

  • Degree in a related subject area.
  • Experience with 2‑D or 3‑D clinical imaging.
  • Experience using eCRFs, EDC systems, or ePRO platforms.
  • Experience working across multiple clinical sites.
  • Knowledge of research regulations at national level.
  • Prior experience in cancer research and endoscopy.
  • Experience in performing nurse‑led clinics.
  • Prior experience of working with Capsule Sponge device.

  Skills & Competencies – Essential

  • Excellent interpersonal and communication skills (verbal and written).
  • High attention to detail and accuracy in documentation.
  • Ability to work accurately and methodically.
  • Strong clinical judgement with appropriate escalation skills.
  • Confidence working autonomously and within multidisciplinary teams.
  • A team player with the ability to work independently and on own initiative.
  • High level of organisational and time management skills.
  • IT proficiency, including digital imaging, electronic data entry, and MS Office.
  • Ability to maintain confidentiality and comply with GDPR requirements.

  Other Requirements – Essential

  • Full, clean UK driving licence.
  • Willingness to travel and complete overnight stays as required.

  Benefits

  • Bank holidays, plus 25 days annual leave, increasing to 28 after 5 years.
  • Buy & Sell Holidays.
  • Enhanced Maternity and Paternity Leave.
  • 1 Occasion Day each year—your choice of your child's first school day, nativity play or your own birthday.
  • Healthshield.
  • Cycle to Work Scheme.
  • Tech Scheme.
  • Electric Car Scheme.
  • Subsidised company events and gatherings.
  • A gift for your birthday.
  • Wellbeing support from our qualified Mental Health First Aiders, as well as via our health scheme.