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Senior Clinical Research Nurse​/Luxury Private Hospital

Job in City of Westminster, Central London, Greater London, England, UK
Listing for: Daytime Healthcare Recruitment Limited
Full Time position
Listed on 2026-01-13
Job specializations:
  • Healthcare
    Clinical Research
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 46010 GBP Yearly GBP 46010.00 YEAR
Job Description & How to Apply Below
Position: Senior Clinical Research Nurse / Luxury Private Hospital
Location: City of Westminster

Daytime Healthcare are assisting a boutique luxury hospital in central London, who are seeking an experienced Clinic Research Nurse to join their team.

Full-time, Monday – Friday 08:00
-17:00 onsite

The clinical trials facility conducts clinical studies to evaluate and determine the potential of new therapeutic agents in asthma, allergy and COPD, but is not limited to research in wider therapeutic areas including urology and gastro-enterology. The facility manages clinical trials from Phase I-IV. The hospital has consolidated its expertise and experience and has a proven track record in performing clinically based pharmacological research to the highest international standards.

They are currently seeking a proactive and enthusiastic Senior Clinical Research Nurse to join our team and support participant recruitment for clinical trials in respiratory and other medical research areas. The Senior Clinical Research Nurse will support in delivering clinical research by helping to set up research studies, carrying out clinical assessments, maintaining high clinical standards and adhering to protocols.

Key Responsibilities:

* Support the delivery of clinical trials in compliance with GCP (Good Clinical Practice) and regulatory requirements.

* Conduct screening, enrolment, and monitoring of study participants, ensuring patient safety and protocol adherence.

* Perform clinical procedures such as venepuncture, ECGs, and drug administration, as required by study protocols.

* Assist in the collection, documentation, and accurate recording of study data in electronic case report forms (eCRFs).

* Collaborate with Principal Investigators (PIs), study coordinators, and multidisciplinary teams to ensure smooth study operations to ensure that the study protocol is correctly implemented and research governance standards are met and maintained.

Apply Today
Position Requirements
10+ Years work experience
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