Clinical Research Nurse: Drive Impactful Trials

Pulse

Leicester

On-site

GBP 34,000 - 41,000

Full time

14 days+
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Job summary

Pulse is seeking a dedicated NMC-registered Clinical Research Nurse to join a fast-paced trials team in Leicester. You will conduct participant visits, data entry into CRFs/eCRFs, and support safety monitoring across therapeutic areas.

Expect strong clinical assessment, excellent communication, and meticulous documentation in an EHR environment. The role requires at least 3 years in clinical research and a valid NMC PIN, with the ability to respond quickly to data queries and emergencies in a

Qualifications

  • NMC PIN is required to practice.
  • A minimum of 3 years' experience in clinical research.
  • Strong clinical experience in a patient-facing environment.
  • Excellent clinical assessment and observational skills.
  • Confident communicator with good organisational abilities.
  • Ability to work effectively in a fast-paced research setting.
  • High attention to detail and accurate documentation.
  • Familiarity with electronic health record systems.

Responsibilities

  • Carry out participant visits, observations, interventions and safety checks per study protocols and SOPs.
  • Complete pre-screen assessments to support patient recruitment.
  • Build positive relationships to improve participant engagement and retention.
  • Record, verify and enter study data into source notes and CRFs/eCRFs.
  • Respond to data queries promptly.
  • Maintain a professional, supportive environment for participants and colleagues.
  • Participate in MDT meetings.
  • Respond confidently in emergencies (e.g., cardiac arrest, anaphylaxis).

Skills

NMC PIN
Clinical research experience
Observation skills
Communication skills
Documentation accuracy
EHR systems

Education

NMC PIN required

Tools

Electronic Health Records (EHR)

Job description

Pulse is seeking a dedicated NMC-registered Clinical Research Nurse to join a fast-paced trials team in Leicester. You will conduct participant visits, data entry into CRFs/eCRFs, and support safety monitoring across therapeutic areas.

Expect strong clinical assessment, excellent communication, and meticulous documentation in an EHR environment. The role requires at least 3 years in clinical research and a valid NMC PIN, with the ability to respond quickly to data queries and emergencies in a

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