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Job overview
The Research Nurse/Clinical Trials Practitioner is an autonomous specialist working within the multi-disciplinary team. The post holder will take responsibility for the co-ordination and management of a clinical research portfolio comprising of in-house, national and international phase II and III clinical trials in hematological malignancies.
Responsibilities will include education of patients and colleagues, coordination of care of patients on trials, collection and preparation of biological samples, collection of trial data and monitoring of the expected and unexpected side effects of drugs and other treatment modalities. The post holder will be expected to develop specialized skills and knowledge relating to the conduct of clinical trials, the therapies and the relevant disease sites. The post holder will be expected to have sufficient skills to enable patients to make informed choices concerning their involvement in clinical trials by providing advice and information and acting as the patient’s advocate.
The post is clinically based to support research in haematological malignancies, and post holders will be expected to provide cross cover for members of the team.
If you would like further information, please contact Leigh Wood [email protected]
Main duties of the job
- To coordinate and conduct in-house, commercial and non-commercial national and international Phase I, II and III clinical trials.. • Be accountable for the documentation of trial data according to ICH GCP guidelines. • Appling critical appraisal skills in evaluating research protocols. • Demonstrates autonomy as well as the ability to collaborate within a multidisciplinary healthcare team in identifying and meeting the needs of the patient and his/her family during various stages of the healthcare continuum. • Coordinates and monitors the care of patients on clinical trials • Educates the multidisciplinary team about portfolio of clinical trials. • To act as a primary point of contact for patients in specific trials. • Educates patient and family about clinical trials, including the objectives, scientific rationale, treatment schedule, side effects and follow up plan. • Develops programs of care for patients taking part in clinical trials. • Mentorship to data managers and clinical trial practitioners. • Provides cross cover for other research nurses, trial practitioners, data managers and assistants working in the clinical trials unit as directed by the Clinical Trials Manager. • To take personal responsibility for promoting a safe environment and safe patient care by identifying areas of risk and following the incident, serious incidents and near misses reporting policy and procedure. • Adheres to Trust and Directorate policies, procedures, standards and protocols. • Research nurses to practice at all times and remain up to date professionally in accordance with the NMC code of professional conduct.
Detailed job description and main responsibilities
For the full Person Specification and more information regarding the main responsibilities of this role, please refer to the attached Job Description. Come and be a part of the best NHS trust in England to work for, according to our staff* * UCLH top trust to work at in England - In the most recent NHS staff survey UCLH had the highest percentage of staff who said they would recommend us as a place to work, out of all general acute or acute/community NHS trusts in England – for the third year in a row. UCLH recognises the benefits of flexible working for staff – To find out more, visit: Flexible working. To discover more about what makes UCLH a great place to work, visit: Why Choose UCLH?
Person specification
Experience
Essential
- Post registration nursing experience
- Experience of working with oncology/haematology patients and ability to demonstrate in-depth knowledge of speciality
- Experience of formal/ informal teaching of patients and/or staff
- Demonstrates evidence of professional development
- Experience working as a preceptor/facilitator
Desirable
- Clinical trials experience
Communication
Essential
- Proven ability to communicate effectively in writing
- Proven ability to work effectively under pressure
Skills and Abilities
Essential
- Demonstrates ability to take charge and delegate duties
Specific Requirements
Essential
- Computer literacy
Desirable
- Proven knowledge of ICH GCP guidelines
- Experience of phlebotomy and cannulation
- Experience of administration of chemotherapeutic agents
Knowledge and Qualifications
Essential
- Registered Nurse Part 1, 2,
- Completed/working towards degree in the speciality or related field
Desirable
- Completed/working towards post graduate course in oncology on other related speciality
- Professionally recognised teaching course
Responsibilities towards promoting Equality Diversity and Inclusion
Essential
- E.g., All posts to include Demonstratable understanding of the Equality, Diversity, and Inclusion and/or Knowledge of the NHS obligations under the Equality Act 2010 and the Public Sector Equality Duties (line managers to elaborate depending on the level of the post and to assess this essential criteria at interview)
Ensure the risk of infection to self, colleagues, patients, relatives and visitors is minimised by:
Essential
- Being familiar with, and adhering to Trust policies and guidance on infection prevention and control.
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Applying for this NHS job
This advert is for Research Nurse with University College London Hospitals NHS Foundation Trust in London, London, England. It is listed as a Band 6 Nurse (adult and children) role. The advertised salary is £47,951 - £56,863 Per annum inclusive of HCAS. The contract type is Fixed term: 12 months (Maternity Cover). The application deadline is 03 Aug 2026.
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