Clinical Research Nurse | Guy's and St Thomas' NHS Foundation Trust
| Posting date: | 23 August 2024 |
|---|---|
| Salary: | Not specified |
| Additional salary information: | £42,471 - £50,364 p.a. inc HCA |
| Hours: | Full time |
| Closing date: | 03 October 2024 |
| Location: | London, SE1 9RT |
| Company: | Guys and St Thomas NHS Foundation Trust |
| Job type: | Contract |
| Job reference: | 6592411/196-RD147 |
Summary
Are you dynamic, patient-centered and looking for an exciting challenge?
Why not consider joining the NIHR Clinical Research Facility (CRF) at Guy’s and St. Thomas’ NHS Foundation Trust?
We have a fantastic development opportunity for a Band 6 or experienced Band 5 nurse to start or continue developing clinical research skills. Previous experience of clinical research projects and SACT competency is desirable. You will need to be a team player and effective at managing your own time.
The role is a combination of clinical and research responsibilities delivered within a diverse portfolio. You will be a point of contact for study principal investigators, sponsors and patients. This means effective communication and team working skills are essential.
To meet the needs of the service you will be required to work at two of our Units – the Guy’s Phase I Unit and the St. Thomas’ Cardiometabolic Unit.
Your work patterns will be agreed with your Line Manager. You will be expected to work shift patterns necessary to ensure patient safety and
delivery of clinical trials.Work patterns will include day shifts, including early and late shifts. There will also be some night duties and
weekends as required.
Assess, plan, implement, and evaluate expert research nursing care and provide support to patients attending the Department who have been or
have the potential to be recruited onto a clinical trial programme. The Research Nurse will play a key role in ensuring that any research
undertaken within the department safeguards the well being of the patients and is conducted according to Good Clinical Practice (GCP) and the Medicines for Human Use (Clinical Trial) Regulations 2004 and Amended Regulations 2006. In conjunction with the other members of the team, facilitate the production of good quality of research.
The research nurse will facilitate and aid in the recruitment of patients to ensure high quality clinical studies and trials which will require the nurse
to work flexibly across the disciplines to ensure the successful working of the clinical research facility. They will also act as a patient advocate
providing support and assistance as required and assist in the co-ordination and management of a portfolio of early phase translational clinical research.
The post holder will take responsibility for supervising the safe administration of experimental therapies, and for monitoring the expected and unexpected side effects of drugs and other treatment modalities used in these trials.
The National Institute of Health Research (NIHR) Clinical Research Facility (CRF) for Experimental Medicine at Guy’s and St Thomas’ NHS
Foundation Trust provides state of the art facilitates and world-leading expertise to support the NHS, universities and industry in conducting
ground breaking experimental medicine studies.
The R&D Department employs a range of senior managers, technical managers, researchers, research support staff, research nurses and administrative staff. Based in the Tower Wing at Guy’s Hospital, this diverse department has the breadth of knowledge and skills to ensure that this high level of research activity and associated research processes are managed smoothly, efficiently and collaboratively.
The Clinical Research Facility is comprised of five units located at our sites at Guys, St. Thomas' and the Royal Bromptom.
With MHRA Phase I accreditation for our Guy’s CRF unit, we are uniquely placed to deliver Phase I commercial and non-commercial patient
focused studies. Our CRF is the only one in the UK with embedded Advanced Therapies Manufacturing (GMP) and immune monitoring platforms.
Clinical
• Carry out planned care required by the clinical trials protocol for a group of volunteers without direct supervision.
• Ensure the assessment, planning, implementation and evaluation of evidence based, individualized patient/volunteer care.
• Responsible for recruiting to, and following up, patients within studies. This includes both randomized clinical trials and other high
quality clinical studies. The role will involve working closely with multidisciplinary clinical teams
• Act as a patient advocate enabling patients to make informed choices concerning their involvement in the clinical trials and ensuring advice and information is provided.
• Ensure there is sufficient skill mix of staff for patient safety during clinical trials and ensuring that they are carried out within the Trust
and Centre's policies and clinical trial protocol.
• Assist in clinical trials including venepuncture and cannulation of volunteers when necessary ensuring that they are carried out within the Trust’s policies, research governance , Medicines for Human Use ( Clinical Trials Regulations ) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP) and Data Protection Act.
• Undertake clinical tasks such as phlebotomy, analysis of blood specimens, drug administration and clinical observation etc.
Assist and advise staff, both registered and unregistered in the delivery of care to the volunteer.
• Ensure that written informed consent has always been obtained for any treatment provided for, or any sample or data taken from a
Volunteer which will form part of a research study , in accordance with the Trust research governance arrangements and Medicines for Human Use ( Clinical Trials Regulations ) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP).
• Have responsibility for the correct administration and custody of medicines according to Trust policy.
• Maintain all data and case report forms relating to clinical trials in accordance with the Medicines for Human Use ( Clinical Trials
Regulations ) Incorporating International Conference on Harmonisation of Good Clinical Practice (ICH GCP).
Report any deviation from normal practice to senior staff and implement agreed changes in care programme.
• Deal with concerns raised by volunteers and visitors in a proactive manner and take remedial action as necessary.
• Act as the volunteers advocate
Administration
• Plan, organize and deploy staff according to ability and workload in order to meet participant needs.
• Ensure that nursing practices comply with Trust policies and procedures
• Communicate effectively at all times and maintain a harmonious working environment.
• Maintain a safe environment in accordance with the Health and Safety at Work Act.
• Assist the Nurse Manager in managing incidents, accidents and complaints in accordance with Trust policies and procedures.
Assist in ensuring the availability of resources for volunteer care
Ensure equipment is in good working order, and report appropriately when defective
• Participate in audits, Eg. those undertaken by the Medicines and Health Care Regulatory Authority ( MHRA ), nursing audits and clinical benchmarking exercises, and suggest any change to improve standards
• Ensure the economical use of resources
• Contribute to the overall control of the ward or departmental budget and identify areas where cost improvements can be made.
• Ensure the safe custody of volunteers property in accordance with Trust policies.
• Actively participate in and support the development of the clinical research facility.
• Promote and participate in the implementation of policies within the Centre and to ensure compliance with Trust, Government and EU Directives.
• Maintain accurate documentation in clinical trial documents and patient notes.
• Ensure that clinical trials are effectively archived as required.
Assist in the process of gaining local regulatory committee approval (ethics and R&D approval).
Education and Training
• Assist in the education and support of health care professionals to enable them to care for clinical trial patients and recruit to clinical trials where appropriate.
• Maintain an up to date knowledge of research related topics particularly related to clinical trials.
• Attend local and national meetings as appropriate and as agreed with the local coordination centre.
• Attend regular update sessions at GSTT.
• Assess the needs of volunteers, relatives and carers and provide them with information as requested
• Educate and counsel volunteers, family and those who volunteer for clinical trials before, during and after clinical studies and investigations
• Assist the Charge Nurse in orientating all new staff and students to the ward or department
• Provide teaching and development to the nursing team and students helping them to achieve their learning outcomes
• Act as a role model, mentor and preceptor to the nursing team
Other
• Understand and adhere to Trust policies and procedures.
To maintain patient confidentiality and standards of Good Clinical
• Practice (GCP) at all times
• Maintain NMC registration
This advert closes on Tuesday 17 Sep 2024