
Research Nurse/AHP
- Torquay, Devon
- £31,049-37,796 per year
- Permanent
- Full-time
- Have an understanding of the clinical research team objectives and contribute to their achievement.
- Manage research performance and study timelines of relevant studies.
- Be responsible for the delivery of a clinical trial portfolio.
- Be responsible for the care of research participants and use opportunities to provide health promotion and patient education.
- Work as part of the multidisciplinary team and contribute to the ongoing development of the department.
- Have an awareness of the income stream relevant to Clinical Trials and work within, local and Trust wide financial and budgetary guidelines.
- Relevant Healthcare Degree
- Registered Nurse or Healthcare Professional
- Research Training (e.g. GCP, degree module, informed consent)
- Demonstrable computer literacy: o ECDL qualification or similar ability o Outlook email and calendars o Microsoft Office: creating folders, editing Word documents o Uploading and downloading attachment files o Basic Excel spreadsheets
- Understand the significance of research and the use of validated results to improve practice
- Understanding of data collection and data entry for clinical trials
- Excellent communication skills
- Evidence of continued professional development
- Excellent organisational skills and able to work to tight deadlines
- Ability to work autonomously
- Ability to work within a team and complement group dynamics
- Ability to prioritise and organise own workload
- Flexible and adaptable
- Willingness to undertake any necessary training and development to enhance work performance
- Commitment to openness, honesty and integrity to undertake the role
- Willingness and ability to work across sites including the community if required
- Ability to communicate complex information to patients/carers and members of the MDT
- Venepuncture/Cannulation
- ECG competency
- Knowledge of Research Governance Framework and Good Clinical Practice Guidelines
- Post-graduate qualification in teaching or equivalent
- Experience of Clinical Trials
- Knowledge of Research Governance
- Knowledge of clinical trials and research methodologies
- Using established databases for data entry
- Proven record of meeting targets
- Good listening and counselling skills
- Ability to concentrate for prolonged periods (e.g. data collection and trial protocol) and deal with interruptions
- Relevant Healthcare Degree
- Registered Nurse or Healthcare Professional
- Research Training (e.g. GCP, degree module, informed consent)
- Demonstrable computer literacy: o ECDL qualification or similar ability o Outlook email and calendars o Microsoft Office: creating folders, editing Word documents o Uploading and downloading attachment files o Basic Excel spreadsheets
- Understand the significance of research and the use of validated results to improve practice
- Understanding of data collection and data entry for clinical trials
- Excellent communication skills
- Evidence of continued professional development
- Excellent organisational skills and able to work to tight deadlines
- Ability to work autonomously
- Ability to work within a team and complement group dynamics
- Ability to prioritise and organise own workload
- Flexible and adaptable
- Willingness to undertake any necessary training and development to enhance work performance
- Commitment to openness, honesty and integrity to undertake the role
- Willingness and ability to work across sites including the community if required
- Ability to communicate complex information to patients/carers and members of the MDT
- Venepuncture/Cannulation
- ECG competency
- Knowledge of Research Governance Framework and Good Clinical Practice Guidelines
- Post-graduate qualification in teaching or equivalent
- Experience of Clinical Trials
- Knowledge of Research Governance
- Knowledge of clinical trials and research methodologies
- Using established databases for data entry
- Proven record of meeting targets
- Good listening and counselling skills
- Ability to concentrate for prolonged periods (e.g. data collection and trial protocol) and deal with interruptions