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.