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- Tasks: Support the QA team in managing our Quality Management System and ensure compliance.
- Company: Join Cancer Research UK, the largest independent funder of cancer science worldwide.
- Benefits: Enjoy a competitive salary, generous benefits, and opportunities for personal development.
- Why this job: Make a real impact in the fight against cancer while developing your skills.
- Qualifications: Experience with electronic Quality Management Systems in clinical or pharmaceutical environments.
- Other info: Flexible working environment with a focus on wellbeing and career growth.
The predicted salary is between 21500 - 25500 £ per year.
14 drugs developed. 6 million courses of treatment. Immeasurable lives improved.
£25,000 - £30,000 (+ Benefits)
Reports to: Quality Assurance Manager
Department: Research & Innovation
Contract: Permanent
Hours: Full time 35 hours per week
Location: Stratford, London. Office-based with high flexibility (1-2 days per week in the office).
Visa sponsorship: 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: 24 February :55
If you require more time to apply as part of a reasonable adjustment request, please contact us as soon as possible.
Recruitment process: One stage competency-based interview
Interview date: From the week commencing 9 March 2026
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 fully complete the work history section of the online application form for us to be able to assess you quickly, fairly, and objectively.
At Cancer Research UK, we exist to beat cancer. We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That’s why we’re looking for someone talented, someone who wants to develop their skills, someone like you.
Cancer Research UK is the largest independent, non-commercial funder of cancer science worldwide. Our Centre for Drug Development (CDD) is the world’s only charity-funded drug development facility that delivers pioneering cancer therapies, clinical trials, and biomarker technologies that rival medium-sized pharmaceutical companies, while reflecting our unique strategy as a charity. We sponsor early phase and precision medicine clinical trials in oncology agents spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in. At the heart of our mission, CDD translates today’s science into tomorrow’s medicine by delivering leading cancer therapies to people with cancer.
It is an exciting time for CDD as we move forward with an ambitious new strategy to maximise the global impact of our research to benefit patients. The Quality Assurance (QA) team is essential to our mission by ensuring the execution of our clinical trials is compliant with good clinical practice (GCP), regulatory requirements, and our Standard Operating Procedures (SOPs).
As a Clinical Quality Assurance Assistant, you will play a vital role in supporting the QA team in managing and maintaining our Quality Management System (QMS), providing administrative and document management support across CDD.
If you are an Administrator who has used electronic Quality Management Systems (QMS) in clinical or pharmaceutical (GxP) environments, we’d love for you to join our mission.
What will I be doing?
- Supporting the Quality Assurance (QA) team in managing and maintaining the Quality Management System (QMS) in line with CDD and clinical GCP standards.
- Taking ownership of QMS administrative tasks, including but not limited to:
- User management
- Document lifecycle management.
- Training record management.
- Training staff to effectively and compliantly use the QMS.
- Compiling information required for quarterly metrics reports.
- Assisting the Quality Assurance Manager in preparing and coordinating inspection activities and follow-ups.
- Providing administrative support to the QA team as required.
- Leading archiving activities, ensuring archived records (paper or electronic) are maintained in accordance with defined procedures and regulatory requirements.
What skills will I need?
- Experienced Administrator who has used electronic Quality Management Systems (QMS) in clinical or pharmaceutical (GxP) environments.
- Demonstrable knowledge and practical application of GxP standards.
- Highly computer literate with proficiency in Microsoft Office Suite.
- Strong organisational skills with a track record of effectively planning, prioritising, and managing multiple tasks while adhering to deadlines and maintaining attention to detail.
- Good interpersonal skills with clear verbal and written communication and the ability to build relationships and collaborate with internal and external stakeholders, as well as part of a team.
- Excellent attention to detail and a demonstrated ability to maintain data integrity and accuracy.
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, take positive steps in your career and achieve your personal wellbeing goals.
You can explore our benefits by visiting our careers web page.
Additional Information
For more information about working with us please visit our website or contact us.
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.
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 Quality Assurance Assistant in London employer: Cancer Research UK (CRUK)
Contact Detail:
Cancer Research UK (CRUK) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Quality Assurance Assistant in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for that interview! Research the company, understand their mission, and be ready to discuss how your skills align with their goals. Practise common interview questions and think of examples that showcase your experience.
✨Tip Number 3
Follow up after your interview! A quick thank-you email can go a long way in showing your enthusiasm for the role. It’s also a chance to reiterate why you’re a great fit for the Clinical Quality Assurance Assistant position.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining our mission to beat cancer.
We think you need these skills to ace Clinical Quality Assurance Assistant in London
Some tips for your application 🫡
Be Yourself: When filling out your application, let your personality shine through! We want to get to know the real you, so don’t be afraid to show your passion for quality assurance and how it aligns with our mission.
Tailor Your Experience: Make sure to highlight your experience with electronic Quality Management Systems (QMS) and any relevant GxP knowledge. We’re looking for specific skills that match the role, so be clear about how your background fits!
Follow the Instructions: Remember to complete the work history section of the online application form thoroughly. This is crucial for us to assess your application fairly, as we won’t be looking at CVs until later in the process.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves, and you’ll find all the info you need about the role there too!
How to prepare for a job interview at Cancer Research UK (CRUK)
✨Know Your GxP Standards
Make sure you brush up on Good Practice (GxP) standards before your interview. Being able to discuss how you've applied these standards in previous roles will show that you're not just familiar with the terminology, but that you understand their importance in clinical settings.
✨Showcase Your QMS Experience
Since this role involves managing a Quality Management System (QMS), be ready to share specific examples of how you've used electronic QMS in past positions. Highlight any administrative tasks you've handled and how you ensured compliance with regulatory requirements.
✨Demonstrate Strong Organisational Skills
Prepare to discuss how you manage multiple tasks and deadlines. Use real-life examples to illustrate your organisational skills, especially in high-pressure environments. This will help convey your ability to thrive in a dynamic setting like Cancer Research UK.
✨Embody the Organisation's Values
Familiarise yourself with Cancer Research UK's values: Bold, Credible, Human, and Together. Think of ways you've demonstrated these values in your work or personal life, and be ready to share those stories during the interview to show you're a great cultural fit.
