Clinical Research Nurse
4 weeks ago
Job Summary
Research Nurse/AHP
An exciting opportunity has arisen for a motivated and enthusiastic Research Nurse/AHP to join our experienced Research Team at Torbay and South Devon NHS Foundation Trust.
The Research Team are passionate about improving patient care and health outcomes through observational and interventional clinical trials.
As a Research Nurse/AHP, you will be responsible for data collection and supporting the team with recruitment into trials. You will work closely with the multi-disciplinary team to ensure the successful delivery of clinical trials.
This is an excellent opportunity for those who wish to start a career in clinical research. Training will be provided for research-specific procedures.
Main Duties of the Job
- Be responsible for the delivery of a clinical trial portfolio.
- Manage research performance and study timelines of relevant studies.
- Have an understanding of the clinical research team objectives and contribute to their achievement.
- 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.
Responsibility for Supervision, Leadership and Management
- Have an awareness of the income stream relevant to Clinical Trials and work within local and Trust-wide financial and budgetary guidelines.
About Us
The clinical research delivery team recruits participants from across the organisation into commercial and non-commercial clinical trials and research. We support research in a variety of clinical specialties and departments. We provide clinical research expertise from setting up studies with the clinical service through to informed consent, trial treatments and interventions and study follow-up.
We use a range of clinical database systems to ensure high-quality clinical data collection. The team supports the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines and provides assurance that the rights, safety, and well-being of trial participants are protected.
Person Specification
Qualifications and Training
- Relevant Healthcare Degree
- Registered Nurse or Healthcare Professional
Knowledge and Experience
- Demonstrable computer literacy: ECDL qualification or similar ability, Outlook email and calendars, Microsoft Office: creating folders, editing Word documents, uploading and downloading attachment files, 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
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