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Research Nurse/Practitioner
2 months ago
We are seeking a highly skilled and motivated Research Nurse/Practitioner to join our dynamic Neurology Research Team at University Hospitals Plymouth NHS Trust. As a key member of our team, you will play a vital role in supporting the safe conduct of research in accordance with the Research Governance Framework and Good Clinical Practice guidelines.
Key Responsibilities- Leadership
- Contribute to the achievement of the clinical research team work-plan.
- Manage research performance and study timelines of relevant studies.
- Collaborate with other Trusts and organizations within the region to improve research delivery.
- Stay up-to-date with research management issues through liaison with other Research Specialists/Team leaders and link with national networks.
- Provide relevant supervision and mentorship to members of staff and students.
- Research
- Be responsible for the delivery of a clinical trial portfolio relevant to the specialty.
- Ensure that the delivery of studies meet requirements with regards to the Department of Health's Research Governance Framework for Health & Social Care and the EU Clinical Trials Directive by implementing quality systems.
- Participate in Good Clinical Practice (GCP) training.
- Contribute to the Expression of Interest/Study Selection process for the relevant specialty.
- Contribute to study set up, recruitment planning, and study delivery.
- Lead forward and contribute to Patient and Public involvement activities.
- Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies.
- Coordinate and run study visits, including off-site visits, while adhering to the lone worker policy.
- Work with other departments within the Trust to ensure that trial-specific investigations and procedures are undertaken as required by the trial protocol.
- Contribute to the accurate costing for clinical trials.
- Ensure clear, accurate, and concise records are kept for research projects in accordance with all regulatory requirements, including the Data Protection Act.
- Ensure that data is transcribed accurately where required and assist with the maintenance of the Trial Master File.
- Respond to data queries generated by the study coordinating team within a timely manner.
- Ensure the recording and reporting of adverse and serious adverse events that occur while the participant is in the clinical trial.
- Assess and evaluate the progress of ongoing clinical trials for which the post-holder has responsibility.
- Escalate ongoing study performance issues to the Senior Research Nurse or Team Lead.
- Cooperate with external and internal audit, data monitoring, and quality assurance by working with R&D, sponsors, study monitors, and external bodies.
- Assist in study close-down and the preparation of results of research for presentation as posters, abstracts, papers, or scientific presentations.
- Clinical & Professional
- Be responsible for the care of research participants within the relevant sphere of practice.
- Use relevant clinical knowledge to screen and identify patients suitable for clinical research.
- Act as a resource and role model for all aspects of Research Clinical Practice.
- Undertake all mandatory training and take part in personal development reviews.
- Ensure the environment is suitable for patient care and research processes.
- Demonstrate professional development and an in-depth knowledge of current clinical and research practice.
- Provide ongoing advice and information to patients and their carers/families regarding their participation in clinical research.
- Where appropriate, receive and document written informed consent from research subjects.
- Be responsible for the safe and accurate collection of research data through clinical procedures.
- Centrifuge, process, track, and ship samples in line with protocol requirements.
- Ensure the safe administration of any treatments and drugs given within the context of a clinical trial.
- Monitor treatment toxicity/side effects and initiate changes to treatment as required by the protocol.
- Ensure accurate patient trial documentation, including the use of electronic data capture systems.
- Refer to other specialists as required to provide optimal care of the participant.
- Contribute to the monitoring of clinical standards within the research team.
- Treat all persons encountered during the course of duties with respect and courtesy.
- Work within the relevant professional code of conduct, demonstrating accountability for own actions and awareness of own limitations.
- Provide cover for other research nurses/practitioners as required.
- Proactively seek feedback from participants and their families during their research involvement.
- Contribute to Patient and Public Involvement and Engagement activities across the department.
