Band 6 - Research Nurse/Midwife
| Posting date: | 10 September 2025 |
|---|---|
| Salary: | £40,617.00 to £48,778.00 per year |
| Additional salary information: | £40617.00 - £48778.00 a year |
| Hours: | Full time |
| Closing date: | 22 September 2025 |
| Location: | Watford, WD18 0HB |
| Company: | NHS Jobs |
| Job type: | Contract |
| Job reference: | C9360-25-0500 |
Summary
Understand international, national, and local policies and legislation relating to clinical trials. Learn to prepare for external inspections (eg MHRA) and internal audits Register/randomise patients into trial protocols Learn to extract clinical data from patients casenotes and transfer the data into the trial Case Report Forms Assist in accurate and complete data collection, updating and maintenance of databases and computerised systems. Take responsibility for filing and safe storage of clinical trials data sheets and for sending to Clinical Trials Units as appropriate Help to deliver, and manage clinical trials, establishing and maintaining channels of communication amongst staff and departments to ensure policies and protocols are understood and adhered to. Understand the role of clinical trials units and liaise with units as necessary Attend and participate in unit meetings and seminars Adequate training to Level 3 safeguarding To facilitate the informed consent process and Liaise with clinical research study personnel outside the hospital as necessary Communicate effectively with participants, the research team and other professional as appropriate to ensure that the trials protocol and SOPs are adhered to To facilitate the informed consent process to ensure the potential research participant (and family) fully understands the nature of the clinical trial/study. To co-ordinate the care of your own caseload of clinical research study participants To comply with and participate in the Trusts framework of clinical governance within the ward or department area, seeking advice or guidance where necessary To ensure that clinical research study recruitment records are accurately maintained, and staff informed of the progress of clinical studies Able to travel to other sites