Research Nurse - BAND 6 inSutton inSutton PUBLISHED FRI 22 NOV 2024

Band 6: £40,701 to £48,054 a year per annum incl. HCAS (PRO RATA for Part Time)  FIXEDTERM 
CANCER HEAD AND NECK CANCER NHS
Opportunity to work in one of the largest and most respected Head and Neck oncology research teams in Europe.
Contribute to pioneering research in the treatment and care of recurrent head and neck cancers, helping to set international standards.
Engage directly with patients as their keyworker, ensuring high standards of care and communication throughout their clinical trial experience.
Possibility to develop professionally in an environment at the forefront of innovation and medical research.
Work collaboratively with multidisciplinary teams and principal investigators, enhancing teamwork and communication skills.
Fixed-term position provides a chance to focus intensively on research without long-term commitments, after which you can assess further career opportunities.
Flexibility in working hours (minimum of 30 hours per week), promoting a healthy work-life balance.
The Royal Marsden NHS Foundation Trust is seeking a Band 6 Research Nurse to join their Head and Neck Research team in Sutton for a fixed-term position of 12 months, requiring a minimum of 30 hours per week. The successful candidate will be integral to managing various head and neck oncology studies, serving as a keyworker for patients enrolled in clinical trials. Responsibilities will include coordinating patient care, recruitment, education, and monitoring, while ensuring adherence to good clinical practice (GCP) standards. The position offers an opportunity to contribute to groundbreaking research in one of Europe's leading head and neck cancer units and engage in ongoing professional development within a supportive environment.

In collaboration with senior nursing staff and the multidisciplinary team, the Research Nurse will facilitate trial processes by coordinating patient investigations, monitoring treatment, and accurately recording data in line with trial protocols. Additional duties involve participating in the design of research documentation and ensuring patients receive comprehensive information and support throughout their clinical trial experience.

 


Locations are approximate. Learn more