Clinical Trials Research Nurse
| Dyddiad hysbysebu: | 23 Gorffennaf 2025 |
|---|---|
| Cyflog: | £39,205.00 i £47,084.00 bob blwyddyn |
| Gwybodaeth ychwanegol am y cyflog: | £39205.00 - £47084.00 a year |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 05 Awst 2025 |
| Lleoliad: | Harlow, CM20 1QX |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | C9292-25-0302 |
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Responsible for the day to day co-ordination, management and nursing of patients and data relating to research projects being undertaken in the department using specific and predetermined trial protocols Act as a primary point of contact for patients taking part in a clinical trial Contribute to the management of the local portfolio of clinical trials Ensure that clinical trial protocols are adhered to Work in accordance to Good Clinical Practice (GCP) and research governance framework standards for clinical trials Facilitate the informed consent process of patients into clinical trials. Providing detailed information to patients to enable them to make an informed decision as to whether they wish to participate in a particular research project Liaise with sponsors/CRAs and or monitors during the conduct of a trial on behalf of the department Supply data as required to the Lead Research Nurse, R&D Manager, EoE RRDN and other approved bodies regarding the progress of clinical trials Maintenance of trial master files taking responsibility for the day to day project administration and document control Identify barriers to recruitment into trials and ensure that the Lead Research Nurse, R&D Manager, EoE RRDN and other approved bodies are aware of them and to support/actions plans as required Provide support for colleagues in their absence Submission of expressions of interest, site feasibilities and local feasibilities Contribute to the planning and acquisition of required resources to undertake clinical research studies to the appropriate standards Ensure that clinical trial recruitment records are accurately maintained Ensure that completed/closed clinical trials are effectively and efficiently archived as per local standards