Main area: Liver Research
Grade: NHS AfC: Band 6
Contract: 12 months (Fixed Term Contract)
Hours: Full time - 37.5 hours per week (Flexible as per service needs)
Job ref: 213-CORP-6832217
Employer: King's College Hospital NHS Foundation Trust
Employer type: NHS
Site: Denmark Hill
Town: London
Salary: £44,806 - £53,134 per annum inc HCA's
Salary period: Yearly
Closing: Today at 23:59
Job overview
An exciting opportunity has become available with the vibrant Liver Research Team at King's College Hospital for a band 6 clinical research nurse. As a member of the Liver Research team, you will be based at King's College Hospital, Denmark Hill. The Liver Research team at the Institute of Liver Studies in King's College Hospital has an impressive portfolio that covers a wide range of studies, including observational cohort studies and interventional trials (phase 1-3) for various liver diseases. The team has gained a reputation for excellence in research delivery. We are looking for a highly motivated and experienced clinical research nurse to join our team. In this role, you will be responsible for coordinating and conducting clinical research activities, such as participant recruitment, data collection and analysis, and ensuring compliance with study protocols and regulatory requirements. To be successful in this role, you should have a proven track record in clinical research, including experience in various research methodologies and a strong understanding of Good Clinical Practice guidelines. Excellent communication and interpersonal skills are essential as you will be working with a diverse range of individuals, including patients, researchers, and industry partners. Main duties of the job
You will be part of the team of liver research nurses to deliver the non-commercial trials and commercial trials within the portfolio, in accordance with the principles of GCP. This will include important trials with a national profile in liver diseases that are both challenging and interesting. The successful candidate will be expected to appropriately manage participants throughout the research pathway, as well as assume administrative responsibility for allocated projects. This will include study and data management activities, with close supervision by the senior research nurse. You will interact with all relevant members of the multidisciplinary team to ensure that all research-related activity is undertaken with patient safety as a key priority and that all projects are delivered efficiently, with adherence to time and target. Excellent communication skills and willingness to learn are essential qualities in the successful applicant. Knowledge of related disease is desirable. For this post you must demonstrate the ability to manage your own workload; understand clinical trial activity and GCP and be able to complete trial documentation accurately and in a timely manner. Working for our organisation
King’s College Hospital NHS Foundation Trust is one of the UK’s largest and busiest teaching Trusts with a turnover of c£1 billion, 1.5 million patient contacts a year and more than 15,000 staff based across South East London. The Trust provides a full range of local and specialist services across its five sites. The trust-wide strategy of Strong Roots, Global Reach is our Vision to be BOLD, Brilliant people, Outstanding care, Leaders in Research, Innovation and Education, Diversity, Equality and Inclusion at the heart of everything we do. We are at a pivotal point in our history and we require individuals who are ready to join a highly professional team and make a real, lasting difference to our patients and our people. Detailed job description and main responsibilities
Clinical Responsibilities Work in conjunction with the Senior Research Nurse/Clinical Trials Coordinator to manage a caseload of patients, whilst working as part of a multidisciplinary team. Maintain effective communication with patients, carers and professionals to ensure service delivery. Assist in screening patients suitable for entry into clinical trials, which may include attending clinics and Multidisciplinary Team (MDT) meetings. Identify patients suitable for entry into clinical trials by attending clinics (screening notes/consultant referral) and MDT meetings. With other members of the healthcare team, ensure patients are fully informed prior to entry in any clinical trial programme. Assist in consenting, randomising, and allocating treatment for patients. Evaluate patient eligibility for clinical trial entry, coordinating pre-study tests, obtaining results and arranging appropriate appointments according to trial protocol. Act as a resource and support to patients and their relatives, explaining practical aspects of clinical trials, assisting and supporting local nursing teams. Coordinate the collection of any blood samples required as part of the clinical trials and ensure safe and appropriate storage of specimens, in conjunction with local nursing teams. Support the administration of trial drugs (commensurate with education and training), reporting any unusual side effects in association with local nursing teams. Maintain adequate patient records and ensure all relevant information is documented in the patient’s medical and nursing notes. Responsible for accurate completion of Case Report Forms (CRFs). Responsible for the collection, coordination, and computerization of data generated from the clinical trials. Provide continuity of care for patients and their carers throughout the trial programme. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. If appropriately trained, keep up to date with current practices for cannulation, phlebotomy and care of patients with Central Venous Access lines. Act as a resource for liver-based research. Portfolio Management and Development Assist in the review of trial protocols and identify resource implications for the site. Set up and maintain the TMF/ISF with essential documents. Liaise with and assist the medical team/sponsor organisation in on-study treatment and follow up of patients. Ensure CRFs are completed accurately and in a timely manner. Ensure SAEs are recorded and reported in accordance with the protocol and/or sponsor’s SOP. For network trials, ensure that accrual data is uploaded onto the NIHR CRN portal using the EDGE clinical trials database and provide information for invoices where appropriate. Liaise with other departments and wards at the site/s to promote a good working environment, integration of research, and open channels of communication. Inform appropriate medical personnel and departments of the portfolio of clinical trials. Participate in the presentation of research findings within the Clinical Research Network South London and outside agencies as appropriate. Report adverse incidents and near misses via the Trust’s online incident reporting form. Coordinate multi-centre trials (where appropriate) with the Kings Health Partners Clinical Trials Office (KHP CTO). Training and Development Attend the KHP CTO, NIHR CRN and CRN South London training programmes and other relevant education and training days/programmes as appropriate. Attend investigator/initiation meetings and conferences when required. Maintain awareness of current advances in hepatology treatments, research, and nursing practice to maintain high standards of care for Nurse trial patients. Disseminate research by assisting in the preparation of posters/research papers for meetings, conferences, and publications. Also circulate trial information and carry out presentations locally. Person specification
Education / Qualification
Nursing Degree Adult RN Evidence of continuous personal, professional and academic development Research Experience
Previous clinical research experience Previous post-registration/post-graduate experience within the Liver department Knowledge and experience of handling complex relationships Skills and competencies
Understanding of Regulatory requirements pertaining to trials Excellent communication and interpersonal skills Ability to perform basic clinical skills (obtaining vital signs measurements) Ability to perform venepuncture and cannulation Report writing and presentational skills Ability to work across boundaries, integrating with multidisciplinary staff in relation to clinical trials You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Name: Anice Sundararaj Job title: Research Matron (Liver & Gastroenterology) Email address: anice.sundararaj@nhs.net Telephone number: 02032992038
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An exciting opportunity has become available with the vibrant Liver Research Team at King's College Hospital for a band 6 clinical research nurse. As a member of the Liver Research team, you will be based at King's College Hospital, Denmark Hill. The Liver Research team at the Institute of Liver Studies in King's College Hospital has an impressive portfolio that covers a wide range of studies, including observational cohort studies and interventional trials (phase 1-3) for various liver diseases. The team has gained a reputation for excellence in research delivery. We are looking for a highly motivated and experienced clinical research nurse to join our team. In this role, you will be responsible for coordinating and conducting clinical research activities, such as participant recruitment, data collection and analysis, and ensuring compliance with study protocols and regulatory requirements. To be successful in this role, you should have a proven track record in clinical research, including experience in various research methodologies and a strong understanding of Good Clinical Practice guidelines. Excellent communication and interpersonal skills are essential as you will be working with a diverse range of individuals, including patients, researchers, and industry partners. Main duties of the job
You will be part of the team of liver research nurses to deliver the non-commercial trials and commercial trials within the portfolio, in accordance with the principles of GCP. This will include important trials with a national profile in liver diseases that are both challenging and interesting. The successful candidate will be expected to appropriately manage participants throughout the research pathway, as well as assume administrative responsibility for allocated projects. This will include study and data management activities, with close supervision by the senior research nurse. You will interact with all relevant members of the multidisciplinary team to ensure that all research-related activity is undertaken with patient safety as a key priority and that all projects are delivered efficiently, with adherence to time and target. Excellent communication skills and willingness to learn are essential qualities in the successful applicant. Knowledge of related disease is desirable. For this post you must demonstrate the ability to manage your own workload; understand clinical trial activity and GCP and be able to complete trial documentation accurately and in a timely manner. Working for our organisation
King’s College Hospital NHS Foundation Trust is one of the UK’s largest and busiest teaching Trusts with a turnover of c£1 billion, 1.5 million patient contacts a year and more than 15,000 staff based across South East London. The Trust provides a full range of local and specialist services across its five sites. The trust-wide strategy of Strong Roots, Global Reach is our Vision to be BOLD, Brilliant people, Outstanding care, Leaders in Research, Innovation and Education, Diversity, Equality and Inclusion at the heart of everything we do. We are at a pivotal point in our history and we require individuals who are ready to join a highly professional team and make a real, lasting difference to our patients and our people. Detailed job description and main responsibilities
Clinical Responsibilities Work in conjunction with the Senior Research Nurse/Clinical Trials Coordinator to manage a caseload of patients, whilst working as part of a multidisciplinary team. Maintain effective communication with patients, carers and professionals to ensure service delivery. Assist in screening patients suitable for entry into clinical trials, which may include attending clinics and Multidisciplinary Team (MDT) meetings. Identify patients suitable for entry into clinical trials by attending clinics (screening notes/consultant referral) and MDT meetings. With other members of the healthcare team, ensure patients are fully informed prior to entry in any clinical trial programme. Assist in consenting, randomising, and allocating treatment for patients. Evaluate patient eligibility for clinical trial entry, coordinating pre-study tests, obtaining results and arranging appropriate appointments according to trial protocol. Act as a resource and support to patients and their relatives, explaining practical aspects of clinical trials, assisting and supporting local nursing teams. Coordinate the collection of any blood samples required as part of the clinical trials and ensure safe and appropriate storage of specimens, in conjunction with local nursing teams. Support the administration of trial drugs (commensurate with education and training), reporting any unusual side effects in association with local nursing teams. Maintain adequate patient records and ensure all relevant information is documented in the patient’s medical and nursing notes. Responsible for accurate completion of Case Report Forms (CRFs). Responsible for the collection, coordination, and computerization of data generated from the clinical trials. Provide continuity of care for patients and their carers throughout the trial programme. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. If appropriately trained, keep up to date with current practices for cannulation, phlebotomy and care of patients with Central Venous Access lines. Act as a resource for liver-based research. Portfolio Management and Development Assist in the review of trial protocols and identify resource implications for the site. Set up and maintain the TMF/ISF with essential documents. Liaise with and assist the medical team/sponsor organisation in on-study treatment and follow up of patients. Ensure CRFs are completed accurately and in a timely manner. Ensure SAEs are recorded and reported in accordance with the protocol and/or sponsor’s SOP. For network trials, ensure that accrual data is uploaded onto the NIHR CRN portal using the EDGE clinical trials database and provide information for invoices where appropriate. Liaise with other departments and wards at the site/s to promote a good working environment, integration of research, and open channels of communication. Inform appropriate medical personnel and departments of the portfolio of clinical trials. Participate in the presentation of research findings within the Clinical Research Network South London and outside agencies as appropriate. Report adverse incidents and near misses via the Trust’s online incident reporting form. Coordinate multi-centre trials (where appropriate) with the Kings Health Partners Clinical Trials Office (KHP CTO). Training and Development Attend the KHP CTO, NIHR CRN and CRN South London training programmes and other relevant education and training days/programmes as appropriate. Attend investigator/initiation meetings and conferences when required. Maintain awareness of current advances in hepatology treatments, research, and nursing practice to maintain high standards of care for Nurse trial patients. Disseminate research by assisting in the preparation of posters/research papers for meetings, conferences, and publications. Also circulate trial information and carry out presentations locally. Person specification
Education / Qualification
Nursing Degree Adult RN Evidence of continuous personal, professional and academic development Research Experience
Previous clinical research experience Previous post-registration/post-graduate experience within the Liver department Knowledge and experience of handling complex relationships Skills and competencies
Understanding of Regulatory requirements pertaining to trials Excellent communication and interpersonal skills Ability to perform basic clinical skills (obtaining vital signs measurements) Ability to perform venepuncture and cannulation Report writing and presentational skills Ability to work across boundaries, integrating with multidisciplinary staff in relation to clinical trials You must have appropriate UK professional registration. This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service. Name: Anice Sundararaj Job title: Research Matron (Liver & Gastroenterology) Email address: anice.sundararaj@nhs.net Telephone number: 02032992038
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