At a Glance
- Tasks: Lead clinical study teams to ensure successful trial deliverables and compliance.
- Company: Join Cancer Research UK, a pioneering charity in drug development.
- Benefits: Competitive salary, flexible working, and generous benefits package.
- Other info: Dynamic environment with opportunities for personal and professional growth.
- Why this job: Make a real impact in cancer research and help save lives.
- Qualifications: Experience in managing clinical studies, preferably in oncology.
The predicted salary is between 43000 - 58000 € per year.
Overview
Clinical Study Manager
£50,000 - £55,000 plus benefits
Reports to: Senior Research Manager
Directorate: Research & Innovation
Contract: 24 month fixed-term contract
Hours: Full time 35 hours per week (Flexible working requests including 4-day weeks OR compressed hours will be considered)
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.
Please note: You must be eligible to work in the UK to apply for this vacancy. Cancer Research UK is not able to offer visa sponsorship.
Closing date: 1 February 2026 23:55
Recruitment process: Screening call followed by competency-based interview.
Interview date: Interviews will be held mid to late February
At Cancer Research UK, we exist to beat cancer.
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 growing portfolio.
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.
This is an opportunity to work as part of a multidisciplinary project team in a well-structured process driven environment. You’ll have the opportunity to be involved in various stages of clinical trials from set up, recruitment through to closedown.
What will I be doing?
Ensure all trial deliverables are met according to timelines, budget, operational best practices and compliance with Cancer Research UK SOPs, policies, the EU Directive and ICH GCP guidelines
To define and agree the study timelines and milestones in conjunction with the study team for their inclusion into the overall project plan
To write and drive the preparation and review of the clinical study protocol and other study essential documents, according to the relevant SOPs
To identify and assess potential trial sites with relevant members of the study team and decide on suitable sites for the study. To negotiate agreements with NHS trusts, including the negotiation of clinical trial costs
To chair and facilitate study meetings with the internal teams, investigators and other key stakeholders and actively manage team actions, track study progress, and regularly communicate study progress to study team, Project Leader, Senior Research Manager and others as appropriate.
To interact with Investigator sites and the study team to ensure excellence of study conduct, reviewing site performance, protocol deviations, and maintaining awareness of issues raised
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 studies
What are we looking for?
Biological 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 industry
Significant experience in project planning – and the tools used to do it
Excellent 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
Our organisation values are designed to guide all that we do.
Bold: Act with ambition, courage and determination
Credible: Act with rigour and professionalism
Human: Act to have a positive impact on people
Together: Act inclusively and collaboratively
We’re looking for people who can believe in and embody these organisation values and can use them to drive forward progress against our mission to beat cancer.
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.
What will I gain?
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 careers web page.
How do I apply?
We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won’t be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you fairly and objectively.
For more information on this career opportunity please visit our website or contact us at recruitment@cancer.org.uk.
For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Our vision is to create a charity where everyone feels like they belong, benefits from and participates in, the work we do. We actively encourage applications from people of all backgrounds and cultures, in particular those from ethnic minority backgrounds who are currently under-represented.
We want to see every candidate performing at their best throughout the job application process, interview process and whilst at work. We therefore ask you to inform us of any concerns you have or any adjustments you might need to enable this to happen. Please contact recruitment@cancer.org.uk or 020 3469 8400 as soon as possible.
Unfortunately, we are unable to recruit anyone below the age of 18, so that we can protect young people from health & safety and safeguarding risks.
Clinical Study Manager in Dartford employer: Cancer Research UK
At Cancer Research UK, we pride ourselves on being an exceptional employer, offering a supportive and flexible work environment that prioritises employee wellbeing and professional growth. As a Clinical Study Manager in our pioneering Center for Drug Development, you will be part of a dynamic team dedicated to advancing cancer research, with access to generous benefits and opportunities for career development in a collaborative and inclusive culture. Join us in making a meaningful impact on patients' lives while enjoying the flexibility of hybrid working arrangements in the vibrant setting of Stratford, London.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Study Manager in Dartford
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who have experience with oncology trials. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for those interviews! Brush up on your knowledge of ICH GCP and the UK clinical trial environment. We want you to shine when discussing your experience managing clinical studies and how you can contribute to our mission.
✨Tip Number 3
Show us your passion! During interviews, share why you're excited about working in cancer research and how your values align with ours. We love candidates who are bold, credible, human, and collaborative.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the details about our flexible working options and benefits there.
We think you need these skills to ace Clinical Study Manager in Dartford
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your application to highlight how your experience aligns with the Clinical Study Manager role. Use keywords from the job description to show us you understand what we're looking for.
Showcase Your Writing Skills:Since excellent writing skills are a must, take the time to craft clear and concise responses in your application. This is your chance to demonstrate your ability to draft protocols and SOPs effectively.
Be Honest About Your Experience:If you're unsure whether you meet all the criteria, don’t hesitate to apply! We value potential and passion just as much as experience. Share your relevant skills and how they can contribute to our mission.
Apply Through Our Website:For the best chance of success, make sure to submit your application through our website. It’s the easiest way for us to keep track of your application and ensure it gets the attention it deserves!
How to prepare for a job interview at Cancer Research UK
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials, especially in oncology. Familiarise yourself with ICH GCP guidelines and the specific requirements of Cancer Research UK. This will not only help you answer questions confidently but also show that you're genuinely interested in the role.
✨Showcase Your Experience
Prepare to discuss your previous experience managing clinical studies. Be ready to share specific examples where you successfully adhered to timelines and budgets. Highlight any challenges you faced and how you overcame them, as this demonstrates your problem-solving skills.
✨Teamwork Makes the Dream Work
Since this role involves leading multidisciplinary teams, be prepared to talk about your interpersonal skills. Think of examples where you've inspired teamwork or resolved conflicts. This will show that you can motivate others and work collaboratively, which is key for a Clinical Study Manager.
✨Ask Thoughtful Questions
At the end of the interview, don’t forget to ask insightful questions about the team, the DETERMIN E trial, or the organisation's future goals. This shows your enthusiasm for the position and helps you gauge if it's the right fit for you.
