Clinical Research Practitioner or Clinical Research Nurse
| Dyddiad hysbysebu: | 03 Mehefin 2025 |
|---|---|
| Cyflog: | £37,338.00 i £39,405.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £37338.00 - £39405.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 29 Mehefin 2025 |
| Lleoliad: | London, SW3 6NP |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | N0047-25-0017 |
Crynodeb
This post is to work within the Imperial College/Royal Brompton cystic fibrosis (CF) clinical trials group comprising clinicians, academics, allied health professionals and admin/ finance members. The Brompton adult and paediatric CF centres are made up of world leading teams undertaking trials seeking improved treatment for adults and children with CF. The team is part of the UK CF Trust Clinical Trials Accelerator Platform (CTAP; https://www.cysticfibrosis.org.uk/the-work-we-do/clinical-trials-accelerator-platform) and the European CF Society Clinical Trials Network (https://www.ecfs.eu/ctn). Both initiatives provide opportunities for our patients to participate in trials of new, cutting-edge medicines. The post holder will assist the team on global, multicentre interventional and observational studies, in both adults and children, being led by Profs Davies, Simmonds and colleagues. You will be primarily responsible for all matters relating to clinical trial data collection and management, involving direct patient interactions and provision of administrative support for trial-related activities. This role requires the post holder to be able to handle a varied and extensive workload. Training will be provided in all aspects of the role. In this exciting and rewarding role,you willbe at the heart of research into cystic fibrosis. Your responsibilities will include: Identifying and recruiting potential participants for clinical research studies, working closely with patients, families, and clinical teams. Providing compassionate and courteous front-line support to study participants, whether in the clinic or over the phone, ensuring their questions and concerns are handled with professionalism and empathy. Performing and reviewing clinical assessments, including the collection and processing of blood or other biological samples, while always prioritising participant comfort and safety. Maintaining accurate, detailed, and up-to-date records of your findings, in full compliance with local policies, procedures, and governance frameworks. Keeping your knowledge current in the field of cystic fibrosis and clinical research by engaging in regular training and attending national and international conferences, with opportunities to pursue areas of personal interest. Contributing to the writing of research reports and publications, helping to shape the evidence base for future treatments and care.