CPL Life Sciences are currently partnering a global CRO who are actively recruiting two Clinical Research Nurses to support a high-volume early-phase clinical trials unit located at a North-West London hospital site.
This is a contract position from March to July, with potential extension due to peak workload demands.
The role involves working night shifts (3 per week) and supporting multiple early-phase studies across a range of therapy areas.
Key responsibilities include:
• Monitoring trial participants overnight
• Conducting study-specific procedures in accordance with clinical protocols,
• administering investigational medicinal products where required
• Recording observations, and responding to any adverse events.
• You will ensure accurate documentation and compliance with GCP, regulatory, and safety standards, while delivering high-quality patient care in a research environment.
• Candidates must be NMC registered
• Prior exposure to clinical trials or research settings and a strong understanding of clinical protocols.
This role is equivalent to NHS Band 5–6, with a competitive hourly rate available. Applicants working full-time for other CROs cannot be considered due to conflict of interest.
If this is of interest to you then please apply here, or email your CV to sarah.phillips@cpl.com for further information.