Position: Nurse – Clinical Research Nurse
Location: York – on-site
Client: Clinical Trials Organisation
Type: 2-3 months initially
Main Responsibilities
- Oversee and deliver all nursing activities across the full lifecycle of clinical trials, from start-up to close-out, in line with ICH/GCP standards.
- Participate in site initiation visits and maintain up-to-date knowledge of study protocols and amendments.
- Conduct patient interest visits with a strong understanding of study requirements.
- Support patient engagement throughout the trial to maximise retention.
- Accurately collect, verify, and document study data in source notes, CRFs/eCRFs, and related documentation.
- Maintain a professional, welcoming, and supportive environment for patients and staff.
- Manage and resolve data queries promptly and efficiently.
- Respond appropriately to medical or site emergencies and ensure emergency equipment is regularly checked.
- Carry out study-related laboratory procedures when required.
- Ensure full compliance with GDPR, SOPs/COPs, and all regulatory and training requirements.
Main Requirements
- NMC registered nurse with no restrictions to practice (must be verified prior to submission)
- Experience working in a fast-paced clinical environment (e.g. A&E)
- Full driving licence essential
- Able to start at short notice
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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