Clinical Research Nurse
| Dyddiad hysbysebu: | 10 Gorffennaf 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: | 23 Gorffennaf 2025 |
| Lleoliad: | Manchester, M20 4BX |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | C9413-25-0467 |
Crynodeb
DUTIES AND RESPONSIBILITIES: Work autonomously in all areas of practice relating to clinical research. Understand and deliver care in accordance with regulatory approved clinical researchprotocols.Clinical Research Nurse Band 6 - 2 - Updated 26/07/24 Understand the process for obtaining NHS permissions (R&D approval) for conductingclinical trials at site. As project lead, ensure permissions are in place prior to any patientrecruitment. Participate in clinical trial feasibilities and risk assessments of clinical trial protocols. Ensure all clinical trial activities are recorded in appropriate systems in a timely manner. Awareness of trial specific, regional and national targets. Identify and implement strategiesfor recruiting patients to clinical trials ensuring that targets for patient recruitment aredelivered. Delegation and oversight of research related activities to research team members (clinicaland administrative) and ensure compliance with SOPs and ICH/GCP. Arrange and facilitate clinical trial related meetings. Involvement in appropriate financial remunerations for clinical trial activity.Clinical Service and Professional Responsibilities Assimilation of highly complex information relating to clinical trials and communication topatients at a level appropriate to their understanding. Ensure highly sensitive informationis communicated to patients, relatives, and carers regarding prognosis Contribute to the development, implementation, and review of specialist care pathways inconjunction with appropriate personnel. Demonstration of expert knowledge in specialist area to maintain clinical excellence. Demonstrate awareness of divisional and trust strategic objectives including performanceindicators and metrics. Escalation of governance issues impacting on delivery of job purpose. To act as a primary contact point for the clinical trial patients and act as adviser to otherhealth care professionals. Responsibility for maintenance and development of professional knowledge and practiceby attending mandatory and specialist training in accordance with local policy. Ensuring care delivery standards in accordance with trial protocol, local policy, NMC Codeof Practice Conduct and current best practice. Development and maintenance of a high-quality service by: Overseeing the safe administration of all licensed and unlicensed medicinalproducts within the context of a clinical trial. Overseeing assessment and evaluation of treatment toxicities and initiation ofappropriate intervention. Contribute to development of specialist Standard Operating Procedures andguidelines. Provide education and support for non-research staff in the delivery of protocol driventreatment for all patients. Participate in monitoring and audit activities within research team To carry out non-medical prescribing within scope of professional practice and inaccordance with local policies and procedures and national legislation (optional anddepending on clinical service needs).Clinical Research Nurse Band 6 - 3 - Updated 26/07/24Personal Education, Training and Development Maintain professional development whilst evaluating own specialist knowledge andpractice through a process of appraisal and personal development planning. Promote the role of the clinical research nurse as an integral part of the healthcaresystem. Increase and maintain awareness of current advances in cancer treatments, research andnursing practice thereby maintaining the highest standard of care for patients with cancerand implementing evidence-based care by continuing professional development. Participation in trust-wide education programmes and study days. Obtain clinical supervision as appropriate. To keep up to date with departmental, Trust, UK and EU developments for themanagement of clinical research ensuring timely, effective implementation of changes. Attendance at team and divisional meetingStaff Management and Development To Support the Senior Clinical Research Nurse in the induction and continued supervisionof junior members of staff, ensuring compliance with regulatory compliance andlegislation. Support the development of specialist study days within own research team. Assist in the provision of specialist education and training in relation to clinical trials to allkey stakeholders. Disseminate information by attendance and /or presentations at local, national andinternational conferences/meetings Contribute to the development of members of the research team