Clinical Research Nurse - Precision Care in Trials

Pulse; Sheffield; On-site; GBP 34,000 - 41,000; Full time

Job summary

Pulse is seeking a Clinical Research Nurse in Sheffield to deliver high‑quality care within clinical trials. You will carry out participant visits, observations and safety checks in line with study protocols and SOPs.

The role requires a valid NMC PIN and at least 3 years of clinical research experience. You will build relationships with participants, ensure accurate data recording in source notes and CRFs, and work as part of a multidisciplinary team to support recruitment and patient safety.

Qualifications

• Must hold a valid NMC PIN.
• Minimum 3 years of experience in clinical research.
• Strong clinical experience in a patient-facing environment.
• Excellent clinical assessment and observation skills.
• Confident communicator with strong organisational abilities.
• Ability to work effectively in a fast-paced research setting.
• Accurate documentation and high attention to detail.
• Experience with electronic health record systems.

Responsibilities

• Carry out participant visits, observations and safety checks per study protocols and SOPs.
• Perform pre-screen assessments to support recruitment.
• Build relationships to encourage 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.
• Act confidently in emergencies as required.

Skills

Clinical communication

Patient-facing care

Documentation accuracy

Observational skills

Organisational skills

Fast-paced work

Data entry

Electronic health records

Tools

Electronic health records

Job description

Pulse is seeking a Clinical Research Nurse in Sheffield to deliver high‑quality care within clinical trials. You will carry out participant visits, observations and safety checks in line with study protocols and SOPs.

The role requires a valid NMC PIN and at least 3 years of clinical research experience. You will build relationships with participants, ensure accurate data recording in source notes and CRFs, and work as part of a multidisciplinary team to support recruitment and patient safety.