Clinical Research Nurse
| Dyddiad hysbysebu: | 19 Tachwedd 2025 |
|---|---|
| Cyflog: | £38,682.00 i £46,580.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £38682.00 - £46580.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 03 Rhagfyr 2025 |
| Lleoliad: | Peterborough, PE3 9GZ |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9310-25-1004 |
Crynodeb
Please refer to the attached job description and person specification for full details of responsibilities. To identify potential participants from clinical services, community services, university and NHS databases, specialist clinics, third sector organisations, schools and other access routes, for RDN portfolio studies and clinical trials. To work with the clinical teams to map the patient pathway for specific trials, performing cognitive assessments, psychological assessments, ECGs, physical examination and phlebotomy and associated processing. To deliver and promote clinical trials and other research studies within the trust. To ensure day to day practice reflects the highest standards of governance, clinical effectiveness, safety and patient experience. To work collaboratively with other colleagues to ensure all studies are delivered on time and target and are delivered in accordance with the requirements of the study protocol. To safely administer all treatments and medications within the context of a clinical trial To be responsible for accurate and timely completion of case report forms (CRFs). Accurate and timely completion of all study-related activities, electronically and/or in paper format. To undertake all aspects of the study protocol and research pathway, including obtaining informed consent, performing all assessments and cognitive testing and aspects of physical examination, and arranging and undertaking follow-ups. To take and process blood samples required and ensure safe and appropriate storage of specimens. To maintain accurate patient records and ensure all relevant information is documented within the patients medical notes and study source documentation. To support carers through the study process, ensuring those involved are well informed. To facilitate delivery of the study procedures in line with the study protocol and ensure that all travel arrangements, hotels etc. are organised for study participants in advance of their arrival. Please note for this role you will be required to travel independently around the county meeting strict time deadlines. You will need to hold a full UK driving licence* and have use of a vehicle. You cannot use public transport for this role as this is not a reliable form of transport and will not allow you to meet service needs. Please confirm in your application that you meet the specified criteria.