Job summary An exciting opportunity has arisen for a Clinical Trial Research Nurse in the Urology team as part of the Cancer Research Delivery Group (CRDG) at St. Bartholomew's Hospital. We are seeking an enthusiastic individual with high levels of attention to detail and is energised by working in a challenging and fast paced environment. The candidate will need experience in haemato-oncology nursing. Chemotherapy trained and competent is desirable. The candidate will work within a highly effective team and should have good IT and communication skills. Previous experience of working in clinical trials would be advantageous Main duties of the job The Clinical Trials Research Nurse is an independent practitioner working within the multi-disciplinary team. The post holder will take responsibility for the co-ordination and management of all aspects of a clinical research portfolio comprising in-house, national and international clinical trials (in relation to anti-cancer treatment or palliative care, such as chemotherapy, radiotherapy, surgery or supportive care). The post holder willo Coordinate clinical trials according to GCP regulatory requirementso Collaborate with key personnel to ensure the continued care and support for patients involved in clinical trialso Work with a team of research nurses and provide specialised nursing interventions (which may include administration of intravesical treatments and assisting physicians during flexi-cystoscopy)o Accurately and timely complete trial data and documentationo Support Clinical Trial Practitioners and Clinical Trial Assistants (including assistance in delegated responsibilities) About us Barts Health is one of the largest NHS trusts in the country, and one of Britain's leading healthcare providers. The Barts Health group of NHS hospitals is entering an exciting new era on our improvement journey to becoming an outstanding organisation with a world-class clinical reputation. Having lifted ourselves out of special measures, we now have the impetus and breathing space to chart a fresh course in which we are continually striving to improve all our services for patients. Our vision is to be a high-performing group of NHS hospitals, renowned for excellence and innovation, and providing safe and compassionate care to our patients in east London and beyond. That means being a provider of excellent patient safety, known for delivering consistently high standards of harm-free care and always caring for patients in the right place at the right time. It also means being an outstanding place to work, in which our WeCare values and behaviours are visible to all and guide us in how we work together. We strive to live by our WeCare values and are committed to promoting inclusion, where every staff member has a sense of belonging. We value our differences and fully advocate, cultivate and support an inclusive working environment. Date posted 06 March 2025 Pay scheme Agenda for change Band Band 6 Salary £44,806 to £53,134 a year per annum inc Contract Fixed term Duration 12 months Working pattern Full-time Reference number 259-7061819GSS Job locations St Bartholomews Hospital London EC1A 7BE Job description Job responsibilities An exciting opportunity has arisen for a Clinical Trial Research Nurse to work as part of the Cancer Research Delivery Group (CRDG). The Centre is: Generously funded by a joint initiative between the Department of Health and Cancer Research UK Part of a nationwide network of 18 centres of scientific and clinical excellence Aims to drive new anti-cancer treatments to patients Affiliated with the National Cancer Research Network and thus incorporates Phase 1 through to Phase 4 clinical trialsIn bringing together laboratory and clinical patient-based research, our Centre promotes the translational work needed to develop new anti-cancer drugs and diagnostics from the laboratory into clinics and then to test them in early phase clinical trials.The Clinical Trials Research Nurse will support the CECM CRDG portfolio of clinical trials to improve patient recruitment and ensure accurate and timely completion of trial data and documentation. Duties will include identifying potential patients to participate in trials, coordinating trials as per study protocols, collection of clinical data on Case Report Forms (CRFs), and following the principles of Good Clinical Practice (GCP).The successful candidate will have experience of working in an oncology / haematology nursing environment and it would be useful to have chemotherapy training. You must have a good understanding of Good Clinical Practice (GCP) and the regulatory environment that surrounds clinical research and it would be advantageous if you have some experience in clinical research.This is a substantive post on an NHS annual funding cycle. All posts are fulltime, fixed term for one year in the first instance. The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below. Job description Job responsibilities An exciting opportunity has arisen for a Clinical Trial Research Nurse to work as part of the Cancer Research Delivery Group (CRDG). The Centre is: Generously funded by a joint initiative between the Department of Health and Cancer Research UK Part of a nationwide network of 18 centres of scientific and clinical excellence Aims to drive new anti-cancer treatments to patients Affiliated with the National Cancer Research Network and thus incorporates Phase 1 through to Phase 4 clinical trialsIn bringing together laboratory and clinical patient-based research, our Centre promotes the translational work needed to develop new anti-cancer drugs and diagnostics from the laboratory into clinics and then to test them in early phase clinical trials.The Clinical Trials Research Nurse will support the CECM CRDG portfolio of clinical trials to improve patient recruitment and ensure accurate and timely completion of trial data and documentation. Duties will include identifying potential patients to participate in trials, coordinating trials as per study protocols, collection of clinical data on Case Report Forms (CRFs), and following the principles of Good Clinical Practice (GCP).The successful candidate will have experience of working in an oncology / haematology nursing environment and it would be useful to have chemotherapy training. You must have a good understanding of Good Clinical Practice (GCP) and the regulatory environment that surrounds clinical research and it would be advantageous if you have some experience in clinical research.This is a substantive post on an NHS annual funding cycle. All posts are fulltime, fixed term for one year in the first instance. The full job description provides an overview of the key tasks and responsibilities of the role, and the person specification outlines the qualifications, skills, experience, and knowledge required. For both documents, please view the attachment/s below. Person Specification Experience Essential Post registration nursing experience Experience of working with oncology/haematology patients Experience of working as part of a multidisciplinary team Experience of explaining complex concepts to patients in a clear and simplified manner Experience of formal/ informal teaching of patients and staff Desirable Experience of working in a clinical research environment Experience of clinical trial data entry Experience as a nurse in urology Skills Essential Proven effectiveness as working as part of a multidisciplinary team Must demonstrate critical and intelligent attention to detail and high standards of accuracy Ability to carry out essential and appropriate nursing care and procedures Ability to identify deteriorating patients and take appropriate action Demonstrates ability to prioritise workload in order to meet deadlines/milestones Demonstrates ability to work under own initiative Demonstrates ability to take charge and delegate duties Demonstrates evidence of professional development Demonstrates understanding of the importance of audit/quality Proven ability to communicate effectively in writing Proven ability to communicate effectively verbally Proven ability to work effectively under pressure Can prove a basic computer literacy in Windows and IT systems Desirable Previous use of Trials Research Management Software e.g. EDGE Experience of phlebotomy and cannulation Understanding and rising to the challenges in patient recruitment Experience with catheterisation (male / female) Completed training and competencies in the delivery of systemic anti-cancer therapies Knowledge Essential Good knowledge of local and national clinical trial regulations Thorough knowledge and understanding of medical terminology Desirable Proven knowledge of ICH GCP guidelines Qualifications Essential Registered Nurse specialty or related field Desirable Completed/working towards post graduate course in oncology or other related specialty Other Essential Willingness to work flexible hours on occasion Displays enthusiastic nature Person Specification Experience Essential Post registration nursing experience Experience of working with oncology/haematology patients Experience of working as part of a multidisciplinary team Experience of explaining complex concepts to patients in a clear and simplified manner Experience of formal/ informal teaching of patients and staff Desirable Experience of working in a clinical research environment Experience of clinical trial data entry Experience as a nurse in urology Skills Essential Proven effectiveness as working as part of a multidisciplinary team Must demonstrate critical and intelligent attention to detail and high standards of accuracy Ability to carry out essential and appropriate nursing care and procedures Ability to identify deteriorating patients and take appropriate action Demonstrates ability to prioritise workload in order to meet deadlines/milestones Demonstrates ability to work under own initiative Demonstrates ability to take charge and delegate duties Demonstrates evidence of professional development Demonstrates understanding of the importance of audit/quality Proven ability to communicate effectively in writing Proven ability to communicate effectively verbally Proven ability to work effectively under pressure Can prove a basic computer literacy in Windows and IT systems Desirable Previous use of Trials Research Management Software e.g. EDGE Experience of phlebotomy and cannulation Understanding and rising to the challenges in patient recruitment Experience with catheterisation (male / female) Completed training and competencies in the delivery of systemic anti-cancer therapies Knowledge Essential Good knowledge of local and national clinical trial regulations Thorough knowledge and understanding of medical terminology Desirable Proven knowledge of ICH GCP guidelines Qualifications Essential Registered Nurse specialty or related field Desirable Completed/working towards post graduate course in oncology or other related specialty Other Essential Willingness to work flexible hours on occasion Displays enthusiastic nature Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Certificate of Sponsorship Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab). From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab). UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Additional information Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions. Certificate of Sponsorship Applications from job seekers who require current Skilled worker sponsorship to work in the UK are welcome and will be considered alongside all other applications. For further information visit the UK Visas and Immigration website (Opens in a new tab). From 6 April 2017, skilled worker applicants, applying for entry clearance into the UK, have had to present a criminal record certificate from each country they have resided continuously or cumulatively for 12 months or more in the past 10 years. Adult dependants (over 18 years old) are also subject to this requirement. Guidance can be found here Criminal records checks for overseas applicants (Opens in a new tab). UK Registration Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window). Employer details Employer name Barts Health NHS Trust Address St Bartholomews Hospital London EC1A 7BE Employer's website https://www.bartshealth.nhs.uk (Opens in a new tab)