Job Search and Career Advice Platform

Enable job alerts via email!

Clinical Research Nurse

EMS Healthcare

Ipswich

On-site

GBP 60,000 - 80,000

Full time

Yesterday
Be an early applicant

Generate a tailored resume in minutes

Land an interview and earn more. Learn more

Job summary

A healthcare company is seeking a Clinical Research Nurse to join a new observational study in Ipswich. This role involves participant screening, detailed wound assessments, and data collection. The ideal candidate will possess clinical experience in wound care and effective communication skills. The position offers a supportive environment with opportunities for professional development, 25+ days annual leave, a health scheme, and enhanced family leave. Join us to make a significant impact on patient care.

Benefits

25 days annual leave, increasing to 28 after 5 years
Enhanced Maternity and Paternity Leave
Healthshield
Cycle to Work Scheme
Electric Car Scheme

Qualifications

  • Registered Nurse with active NMC registration is essential.
  • Clinical experience in wound care is required.
  • Experience in clinical research is essential.

Responsibilities

  • Screen participants according to criteria.
  • Perform wound examinations and assist investigators.
  • Upload imaging securely and accurately to the central server.

Skills

Excellent interpersonal and communication skills
High attention to detail and accuracy
Strong clinical judgement
IT proficiency including digital imaging

Education

Registered Nurse with active NMC registration
Good Clinical Practice training

Tools

LifeViz® Mini 3-D imaging equipment
Job description

This is an exciting opportunity to join EMS Healthcare on a new observational study, contributing to innovative research within a focused, fixed-site clinical setting.

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.
Person Specification
Qualifications

Essential

  • 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

Desirable

  • Degree in a related subject area
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

Desirable

  • 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

You work hard for us; we work hard for you. It is that simple. And we know, it sounds too good to be true (we hear that a lot). But trust us, this could be the best decision you make.

  • 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; this could be your child’s first day of school, their nativity play, or your own birthday – the choice is yours!
  • Healthshield
  • Cycle to Work Scheme
  • Tech Scheme
  • Electric Car Scheme
  • Subsidised company events and gatherings
  • A gift for your birthday
  • Well being support from our qualified Mental Health First Aiders, as well as via our health scheme

If you want to join us as our Clinical Research Nurse - click apply now!

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.