Senior Clinical Research Nurse
2 weeks ago
About the Role
We are seeking a highly skilled and experienced Clinical Research Nurse to join our team at The Christie NHS FT. As a Clinical Research Nurse, you will play a vital role in the delivery of high-quality clinical research, ensuring that our patients receive the best possible care.
Key Responsibilities
- Work autonomously in all areas of practice relating to clinical research, ensuring that our patients receive the best possible care.
- Understand and deliver care in accordance with regulatory approved clinical research protocols, maintaining the highest standards of patient care.
- Oversee the process for obtaining NHS permissions (R&D approval) for clinical trials within the team, ensuring that all necessary approvals are in place.
- As project lead, ensure that permissions are in place prior to any patient recruitment, ensuring that our patients receive the best possible care.
- Undertake feasibility and risk assessments of clinical trial protocols in conjunction with Team Leader, Principal Investigator, and Senior Clinical Trials Co-ordinator, ensuring that all necessary risks are mitigated.
- Ensure that all clinical trial activities are recorded in appropriate systems in a timely manner, maintaining accurate and up-to-date records.
- Awareness of trial specific, regional, and national targets, ensuring that our team is working towards the same goals.
- Initiate new recruitment strategies for recruiting patients to clinical trials, including engagement with the research network, to ensure that our patients receive the best possible care.
- In conjunction with Team Leader, lead on the delegation of all trial related activities to research team members (clinical and administrative) and ensure compliance with SOPs and ICH/GCP, maintaining the highest standards of patient care.
Personal and Professional Development
- Maintain professional development whilst evaluating own specialist knowledge and practice through a process of appraisal and personal development planning, ensuring that our team is working towards the same goals.
- Promote the role of the clinical research nurse as an integral part of the healthcare system, ensuring that our patients receive the best possible care.
- Increase and maintain awareness of current advances in cancer treatments, research and nursing practice, thereby maintaining the highest standard of care for patients with cancer and implementing evidence-based care by continuing professional development.
- Participation in trust-wide education programs and study days, ensuring that our team is working towards the same goals.
- Obtain clinical supervision as appropriate, ensuring that our team is working towards the same goals.
- To keep up to date with departmental, Trust, UK and EU developments for the management of clinical research, ensuring timely, effective implementation of changes.
- Attendance at team and divisional meetings, ensuring that our team is working towards the same goals.
Staff Management and Development
- In conjunction with the team leader, provide the induction, continued supervision and management of the research teams, ensuring that our team is working towards the same goals.
- In conjunction with the team leader, be responsible for ensuring all members of the research nurse team undergo regular appraisal and support appropriate training and development opportunities in line with role requirements, ensuring that our team is working towards the same goals.
- Lead on the development of specialist study days within own research team, ensuring that our team is working towards the same goals.
- Provide specialist education and training in relation to clinical trials to all key stakeholders, ensuring that our team is working towards the same goals.
- Disseminate information by attendance and/or presentations at local, national and international conferences/meetings, ensuring that our team is working towards the same goals.
- Be responsible for the development of members of the research team, ensuring that our team is working towards the same goals.
EU DIRECTIVE ICH/GCP
All personnel involved in clinical research have a responsibility to ensure that clinical trials are conducted in accordance with the EU Directive and ICH/GCP, maintaining the highest standards of patient care.
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