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- Tasks: Provide expert regulatory guidance for innovative oncology trials and manage Clinical Trial Authorisation applications.
- Company: Join Cancer Research UK, a pioneering charity dedicated to beating cancer.
- Benefits: Enjoy a competitive salary, flexible working, and a supportive environment for personal development.
- Why this job: Make a real impact in the fight against cancer while advancing your career in regulatory affairs.
- Qualifications: Degree in a scientific discipline and experience in regulatory affairs, especially clinical trials.
- Other info: Work in a dynamic team with opportunities for growth and collaboration.
The predicted salary is between 55000 - 60000 £ per year.
11 drugs developed. 6 million courses of treatment. Immeasurable lives improved.
Reports to: Senior Regulatory Affairs Manager (Team Lead)
Directorate: Research & Innovation
Contract: 12 months, Fixed Term Contract
Hours: Full time 35 hours per week
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 to the office typically 4 to 6 times a year, please note that travel expenses to and from the office are not covered. We aim to keep travel minimal and purposeful, ensuring it adds real value to your work and team collaboration.
Closing date: 1st April 2026 23:55pm
Recruitment process: Screening calls followed by Teams Competency Based Interview
Interview date: w/c 20th April 2026
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.
At Cancer Research UK, we exist to beat cancer. Cancer Research UK are looking for an experienced regulatory affairs professional to join our Centre for Drug Development as a Regulatory Affairs Manager. Experience in chemistry, manufacturing and controls (CMC) would be an advantage, but is not essential.
The Cancer Research UK Centre for Drug Development (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.
In this role you’ll be providing expert regulatory advice and support to cross-functional project teams within the CDD, supporting the preclinical development and clinical trials of a varied portfolio of novel oncology products. Any background in CMC can further support the development of regulatory strategies for our trials.
Our regulatory managers are responsible for managing the submission and ongoing maintenance of optimal Clinical Trial Authorisation (CTA) applications both in the UK and EU, ensuring compliance with the current Clinical Trial legislation. This is an excellent opportunity for a regulatory affairs expert to gain valuable experience across a broad range of early-phase oncology trials spanning the UK and Europe. Experience in CMC, particularly within early phase clinical trials would be advantageous.
It is an exciting time for CDD as our teams are working to deliver an ambitious new strategy to maximise the impact of our research to benefit patients - Our project portfolio has recently expanded in size as we move forward with trials both in the UK and EU.
What will you be doing?
- Working in cross-functional project teams, to provide expert regulatory guidance and input to support the project strategy from portfolio entry through to trial completion.
- Advising on CTA documentation requirements, agreeing responsibilities, managing review processes and submission timelines.
- Co-ordinating and submitting optimal Clinical Trial Authorisation (CTA) applications in compliance with CDD standard operating procedures (SOPs) and current UK and EU regulatory agency requirements.
- Leading internal discussions to respond to questions raised, ensuring responses are submitted within the required timeframe.
- Leading the production of the Investigational Medicinal Product Dossier (IMPD) for designated projects, writing sections and liaising with other team members and third-party contacts as appropriate.
- Providing general regulatory advice to CDD (and CRUK) and contributing to the continuous review and improvement of systems and processes, to ensure regulatory compliance and best practice.
What are we looking for?
- Degree in a scientific discipline or equivalent relevant experience.
- Experience of working in regulatory affairs, especially around clinical trials, with any additional CMC expertise considered desirable.
- Ability to apply specialist regulatory knowledge and experience to support the regulatory aspects of early phase drug development in the Charity.
- Experience of writing and reviewing IMPDs and other regulatory documents, including ability to interpret and accurately summarise complex scientific data for inclusion in regulatory packages.
- Able to work independently with minimal supervision, proactively managing own workload and assuming regulatory lead role on designated projects with accountability for regulatory output and associated project deliverables.
- Excellent knowledge of current Clinical Trial Legislation, specifically UK and EU and particularly in relation to first-in-human trials.
- Skilled in assessing and effectively communicating information within project teams and to senior managers.
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.
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. 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 or 0 20 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.
Regulatory Affairs Manager – Oncology Trials (UK/EU CTA) in Edinburgh employer: Cancer Research UK
Contact Detail:
Cancer Research UK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager – Oncology Trials (UK/EU CTA) in Edinburgh
✨Tip Number 1
Network like a pro! Reach out to your connections in the regulatory affairs 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 UK and EU clinical trial legislation. Be ready to discuss how your experience aligns with the role and how you can contribute to our mission at Cancer Research UK.
✨Tip Number 3
Show us your passion! During interviews, share why you’re excited about working in regulatory affairs, particularly in oncology. We want to see that you’re not just looking for a job, but that you genuinely care about making a difference.
✨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 team and contributing to our fight against cancer.
We think you need these skills to ace Regulatory Affairs Manager – Oncology Trials (UK/EU CTA) in Edinburgh
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Regulatory Affairs Manager role. Highlight your relevant experience in regulatory affairs, especially around clinical trials, and any CMC expertise you might have. This shows us that you understand what we're looking for!
Showcase Your Skills: Don’t just list your qualifications; demonstrate how your skills align with our mission to beat cancer. Use specific examples from your past work to illustrate your ability to manage CTA applications and provide regulatory guidance. We love seeing real-world applications of your expertise!
Be Clear and Concise: When filling out the application form, keep your answers clear and to the point. We appreciate straightforward communication, so avoid jargon unless it’s necessary. This will help us assess your fit for the role more easily.
Apply Through Our Website: Remember to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered fairly. Plus, you’ll find all the info you need about the role and our organisation there.
How to prepare for a job interview at Cancer Research UK
✨Know Your Regulatory Stuff
Make sure you brush up on the latest UK and EU Clinical Trial legislation. Familiarise yourself with the specifics of Clinical Trial Authorisation (CTA) applications, as this will be a key focus in your role. Being able to discuss recent changes or trends in regulatory affairs will show that you're not just knowledgeable but also genuinely interested in the field.
✨Showcase Your Experience
Prepare to talk about your previous experience in regulatory affairs, especially around clinical trials. Have specific examples ready that highlight your ability to manage submissions and maintain compliance. If you've worked on Investigational Medicinal Product Dossiers (IMPDs), make sure to mention that too!
✨Team Player Vibes
Since you'll be working in cross-functional project teams, it's important to demonstrate your collaborative skills. Think of examples where you've successfully worked with others to achieve a common goal. Highlight how you communicate effectively within teams and how you handle feedback or differing opinions.
✨Ask Smart Questions
At the end of the interview, don’t forget to ask insightful questions. This could be about the team dynamics, ongoing projects, or how the organisation measures success in regulatory affairs. It shows that you're engaged and thinking ahead about how you can contribute to their mission to beat cancer.