Job Description

An exciting opportunity has arisen for a Clinical Trial Practitioner to work 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 work within a highly effective team and should have good IT and communication skills. Experience in co-ordinating trials involving systemic anti-cancer agents would be desirable.Main duties of the jobThe Clinical Trials Practitioner is an independent practitioner working within the multi-disciplinary team. The post holder will take responsibility for the co-ordination and management of a clinical research portfolio comprising in-house, national and international phase II and III 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 trials. o Accurately and timely complete trial data and documentationWe 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 work within a highly effective team and should have good IT and communication skills. Experience in co-ordinating trials involving systemic anti-cancer agents would be desirable.About usBarts 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 posted28 April 2025Pay schemeAgenda for changeBandBand 5Salaryxc2xa335,964 to xc2xa343,780 a year per annum incContractFixed termDuration12 monthsWorking patternFull-timeReference number259-7174347GSSJob locationsSt Bartholomew's HospitalLondonEC1A 7BEJob descriptionJob responsibilitiesThe 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 descriptionJob responsibilitiesThe 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 SpecificationExperienceEssential

• Significant experience of working in a clinical research environment
• 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
• Experience of clinical trial data entry

• Experience of working with oncology/haematology patients

• Proven effectiveness as working as part of a multidisciplinary team
• Must demonstrate critical and intelligent attention to detail and high standards of accuracy
• 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

• Previous use of Trials Research Management Software e.g. EDGE
• Experience of phlebotomy and cannulation
• Understanding and rising to the challenges in patient recruitment

• Good knowledge of local and national clinical trial regulations
• Proven knowledge of ICH GCP guidelines
• Thorough knowledge and understanding of medical terminology

• Completed degree in biological sciences or equivalent

• Willingness to work flexible hours on occasion
• Displays enthusiastic nature

• Significant experience of working in a clinical research environment
• 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
• Experience of clinical trial data entry

• Experience of working with oncology/haematology patients

• Proven effectiveness as working as part of a multidisciplinary team
• Must demonstrate critical and intelligent attention to detail and high standards of accuracy
• 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

• Previous use of Trials Research Management Software e.g. EDGE
• Experience of phlebotomy and cannulation
• Understanding and rising to the challenges in patient recruitment

• Good knowledge of local and national clinical trial regulations
• Proven knowledge of ICH GCP guidelines
• Thorough knowledge and understanding of medical terminology

• Completed degree in biological sciences or equivalent

• Willingness to work flexible hours on occasion
• Displays enthusiastic nature

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