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Clinical Research Nurse

Job in Stoke-On-Trent, Stoke, Staffordshire, EX39, England, UK
Listing for: Barrington James
Full Time position
Listed on 2026-08-11
Job specializations:
  • Nursing
Job Description & How to Apply Below
Location: Stoke-On-Trent

Senior Clinical Research Nurse

About the Role

We are seeking experienced and motivated Senior Clinical Research Nurses to join a growing clinical research team supporting the delivery of Phase II-IV clinical trials across a variety of therapeutic areas.

Key Responsibilities

  • Coordinate and manage clinical trials from study start-up through to close-out.
  • Read and interpret study protocols, investigator brochures and regulatory documentation.
  • Conduct participant screening, recruitment and informed consent discussions in accordance with GCP guidelines.
  • Perform research visits and protocol-specific clinical assessments.
  • Administer investigational products and monitor participants for adverse events.
  • Manage study randomisation processes and investigational product accountability.
  • Collect, process and manage clinical samples in accordance with study requirements.
  • Maintain accurate source documentation and essential study records.
  • Liaise with investigators, sponsors, CROs and multidisciplinary healthcare teams.
  • Ensure compliance with study protocols, GCP guidelines, SOPs and regulatory requirements.
  • Support site initiation activities, ethics submissions and study close-out processes.
  • Participate in monitoring visits, audits and regulatory inspections.
  • Identify and escalate risks, issues and protocol deviations as appropriate.
  • Contribute to continuous improvement initiatives and research best practices.
  • Undertake additional duties required to support the successful conduct of clinical trials.

Qualifications, Experience & Essential Skills

  • Registered Nurse (NMC).
  • Minimum of 5 years' clinical research experience.
  • Current GCP certification.
  • Experience supporting Phase II-IV clinical trials.
  • Strong understanding of clinical research regulations and study conduct.
  • Excellent communication, organisational and problem-solving skills.
  • High attention to detail and commitment to quality.
  • Ability to work independently and collaboratively within a multidisciplinary team.
  • Compassionate, patient-focused approach to care.
  • Full UK driving licence and willingness to travel between clinical sites when required.

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