.**Integrated planning. Proactive settings. Knowledge that just keeps growing.** **Clinical Study Manager** **Location:** Stratford, London Office-based with high flexibility (1-2 days per week in the office) We’re happy to offer home-based contracts through our flexible working policy. While this role does involve occasional travel—typically 4 to 6 times a year within the London area—please note that travel expenses are not covered. We aim to keep travel minimal and purposeful, ensuring it adds real value to your work and team collaboration. Cancer Research UK are looking for a Clinical Study Manager to join our Center for Drug Development (CDD), leading the multidisciplinary clinical study teams to ensure all clinical trial deliverables are met. This is a 2-year contract to support our platform trial, The CDD is the world's only charity-funded drug development facility. Our pioneering research is driven purely by the goal to see scientific breakthroughs bring benefits to patients sooner. CDD is the sponsor of early phase and precision medicine clinical trials in oncology agents. Our broad portfolio rivals that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in.You might be a Clinical Study Manager/Trial Manager or Clinical Trial Project Manager, with experience working on Oncology trials (ideally early phase but not essential). You might have experience within the NHS, Pharma, Biotech or come from an academic background. Whatever the sector, if you can demonstrate relevant skills in managing clinical trials we would love to hear from you.To write and drive the preparation and review of the clinical study protocol and other study essential documents, according to the relevant SOPs To liaise with the Medical Writing team for the delivery of the clinical study reports To identify best practices, lead or contribute to continual improvement initiatives and implement new procedures for managing clinical studiesBiological Sciences degree or equivalent nursing qualification/experience Experience of managing clinical studies (preferably including early phase oncology) – evidence of successful adherence to study timelines and an understanding of key issues surrounding trial management Strong interpersonal skills with the ability to inspire effective teamwork and motivate members within a matrix system. Resolves conflict as needed. Outstanding knowledge of ICH GCP, the UK clinical trial environment, drug development process and early phase clinical trials relevant to the pharmaceutical/biotech industrySignificant experience in project planning – and the tools used to do itExcellent writing skills to enable drafting and creation of SOPs, protocols, NHS trust agreements and other relevant documents.Strong negotiation skills to enable negotiation of costs and contracts If you’re interested in applying and excited about working with us but are unsure if you have the right skills and experience we’d still love to hear from you.We create a working environment that supports your wellbeing and provide a generous benefits package, a wide range of career and personal development opportunities and high-quality tools. Our policies and processes enable you to improve your work-life balance and take positive steps in your career. You can explore our benefits by visiting our As the world’s largest independent cancer research charity, we conduct research into the prevention, diagnosis and treatment of the disease. Our aim is to see 3 in 4 people survive cancer by 2034 and our staff are integral to achieving that ambition. Cancer Research UK offers you excellent prospects to expand your career as well as the ability to make a real difference to the lives of others. We're always looking for sharp, brave, and collaborative people to join Cancer Research UK and continue to make it a great place to work. Find the career you're looking for and let us change lives together.
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