Research Nurse
NHS Jobs Liverpool
Develop additional clinical skills to meet the needs of individual studies. Act as a resource for other research nurses/HCAs/ admin staff within the research team. Be responsible for the delivery of allocated research studies. Oversee studies allocated to more junior nurses/staff.
Ensure that the delivery of studies meet requirements with regards to the UK policy framework for health and social care research and the EU Clinical Trials Directive by implementing quality systems. Participate in Good Clinical Practice (GCP) training, keeping up to date with any changes in legislation or practice.
Contribute to the Expression of Interest / Study Selection process. Contribute to study set up, recruitment planning and study delivery. Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies.
Work with research teams and the CRN to develop strategies to overcome barriers to recruitment and to solve other problems relating to specific studies. Coordinate and run study visits including off site visits (as needed.) 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 Study Site File Respond to data queries generated by the study coordinating team within a timely manner. Ensure the recording & reporting of adverse and serious adverse events that occur whilst the participant is in the research study to the study co-coordinator/Principal Investigator (PI) and R&D office in line with the study protocol, local policies and regulatory requirements.
Assess and evaluate the progress of on-going studies, maintaining accurate records of the status of studies and providing regular updates to the research team on the status of the studies. This will involve ensuring that the Local Patient Management System (LPMS) EDGE is updated with key study data and validated efficiently.
Discuss on-going study performance issues with the PI. Co-operate with external and internal audit, data monitoring and quality assurance by working with R&D, sponsors, study monitors and external bodies. Assist with study close down and ensure documentation is archived as per study protocol.
Ensure Finance team is informed when invoices are to be sent to study teams and liaise with Finance to ensure costs are received from study teams and CRN. Advocate for research provide education and training on research projects to interested parties as required.
Ensure that the delivery of studies meet requirements with regards to the UK policy framework for health and social care research and the EU Clinical Trials Directive by implementing quality systems. Participate in Good Clinical Practice (GCP) training, keeping up to date with any changes in legislation or practice.
Contribute to the Expression of Interest / Study Selection process. Contribute to study set up, recruitment planning and study delivery. Be responsible for promoting the appropriate referral and recruitment of patients to clinical research studies.
Work with research teams and the CRN to develop strategies to overcome barriers to recruitment and to solve other problems relating to specific studies. Coordinate and run study visits including off site visits (as needed.) 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 Study Site File Respond to data queries generated by the study coordinating team within a timely manner. Ensure the recording & reporting of adverse and serious adverse events that occur whilst the participant is in the research study to the study co-coordinator/Principal Investigator (PI) and R&D office in line with the study protocol, local policies and regulatory requirements.
Assess and evaluate the progress of on-going studies, maintaining accurate records of the status of studies and providing regular updates to the research team on the status of the studies. This will involve ensuring that the Local Patient Management System (LPMS) EDGE is updated with key study data and validated efficiently.
Discuss on-going study performance issues with the PI. Co-operate with external and internal audit, data monitoring and quality assurance by working with R&D, sponsors, study monitors and external bodies. Assist with study close down and ensure documentation is archived as per study protocol.
Ensure Finance team is informed when invoices are to be sent to study teams and liaise with Finance to ensure costs are received from study teams and CRN. Advocate for research provide education and training on research projects to interested parties as required.
Mentor new research nurses and provide clinical support as needed. Whilst the post holder will work within specific research study protocols and guidelines it is essential for the post-holder to work on her/his own initiative, demonstrate a flexible approach to work and to function well as part of the wider Brownlow Team.
Brownlow HealthLiverpool
chronic disease experience) is desirable, but not essential, as this role is also likely to suit an established research nurse who is currently working in secondary care but is looking to transition to a primary care role.
You will work closely with other...
Manchester, 28 mi from Liverpool
Job Title: Senior Research Nurse
Location: Manchester
Salary: £46,148 to £52,809 DOE
Job type: Full Time, Permanent
The Role:
The (NHD) is a register of people in the UK with all types of bleeding disorders started in 1969. Its purpose...
The Christie NHS Foundation TrustManchester, 28 mi from Liverpool
This post presents an exciting opportunity for a highly motivated nurse, interested in helping to improve patient outcomes to join the Head & Neck Research Team as a Band 6 Research Nurse.
The Head & Neck Research Team currently consists of 4...