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  • Job
    Full-time
    Entry Level
  • Research & Development
    Healthcare
  • London

AI generated summary

  • You need enthusiasm, adaptability, excellent communication, attention to detail, and a patient-first approach. Willingness to learn and support patients in trial decisions is essential.
  • You will coordinate patient care in trials, collect samples, administer treatments, monitor side effects, provide patient education, liaise with sponsors, ensure accurate data submission, and mentor new team members.

Requirements

  • We’re looking for someone who is enthusiastic, adaptable, and thrives in a dynamic environment.
  • You’ll need excellent communication skills, a meticulous approach to detail, and the ability to juggle competing priorities — all while putting patients first.
  • You don’t need years of research experience; what matters most is your drive to learn and your commitment to delivering outstanding care.
  • The post holder will work in accordance with the NMC Code of Professional Conduct and relevant professional guidelines, taking responsibility for the coordination and delivery of clinical trials within the Clinical Research Facility (CRF).
  • The post holder will also be expected to develop specialist skills and knowledge related to the conduct of clinical trials, investigational therapies, and the relevant disease areas.
  • They must be able to support patients in making informed decisions about their participation in trials by offering clear advice, information, and advocacy.
  • Please note that while the CRF’s core working hours are 09:00 to 17:00, occasional evening, night, or weekend work may be required to meet the needs of specific studies.

Responsibilities

  • Coordinating the care of patients participating in clinical trials
  • Collecting and preparing biological samples
  • Administering investigational products and experimental agents
  • Monitoring and managing both expected and unexpected side effects of drugs and treatment modalities
  • Providing education and support to patients and their carers
  • Liaising with pharmaceutical companies and other study sponsors as required
  • Ensuring the accurate collection, recording, and submission of research data in line with study protocols and regulatory requirements
  • Deputising for the Senior Research Nurses in their absence
  • Supporting, mentoring, and helping to develop new members of the CRF team

FAQs

What qualifications are required for the Clinical Research Nurse position?

While specific years of research experience are not necessary, a relevant nursing qualification and registration with the NMC are essential. An enthusiasm for research and a commitment to providing outstanding patient care are also important.

What are the core working hours for this role?

The core working hours for the Clinical Research Facility (CRF) are 09:00 to 17:00, although occasional evening, night, or weekend work may be required to meet the needs of specific studies.

Will I receive training in clinical trial processes?

Yes, you will be expected to develop specialist skills and knowledge related to the conduct of clinical trials and investigational therapies, with support provided for your learning and professional development.

Is there a focus on patient interaction in this role?

Yes, the Clinical Research Nurse plays a crucial role in coordinating patient care, providing education and support to patients and their carers, and helping patients make informed decisions about their participation in trials.

What additional responsibilities does the Clinical Research Nurse have?

Additional responsibilities include liaising with pharmaceutical companies and study sponsors, ensuring accurate data collection and submission in line with study protocols, and supporting and mentoring new members of the CRF team.

How do I apply for this position?

Interested candidates should reach out for further details or informal visits by contacting Keenjee Nama, Senior Research Nurse, at keenjee.nama@nhs.net.

What types of studies will I be involved in?

The Clinical Research Nurse will be involved in delivering groundbreaking clinical trials across various disease areas, particularly in women’s health, cancer, neurological, gastrointestinal, and oral disease.

Is UCLH committed to sustainability?

Yes, UCLH is committed to sustainability and has pledged to become a carbon net zero health service, with ambitious targets for reducing direct and indirect emissions.

What kind of support will I have in this role?

As a Clinical Research Nurse at UCLH, you will be supported by a passionate team and provided with the tools to develop your nursing career in a prestigious research hospital.

Will I have to work with pharmaceutical companies?

Yes, part of the role involves liaising with pharmaceutical companies and study sponsors as required for the successful conduct of clinical trials.

UCLH provides first-class acute and specialist services in six hospitals in central London.

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Mission & Purpose

University College London Hospitals (UCLH) NHS Foundation Trust is one of the UK's largest and most renowned healthcare providers. The Trust delivers high-quality patient care across a range of specialties, including cancer, neurology, women’s health, and emergency services. UCLH is committed to clinical excellence, research, and education, aiming to improve health outcomes through innovative treatments and world-class facilities. Their mission is to provide exceptional care and to advance medical knowledge for the benefit of patients and the wider community.