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- Tasks: Write and edit clinical documents to support groundbreaking cancer trials.
- Company: Join Cancer Research UK, a leader in charity-funded drug development.
- Benefits: Enjoy flexible working, a competitive salary, and a supportive environment.
- Why this job: Make a real difference in the fight against cancer while advancing your career.
- Qualifications: Experience in regulatory medical writing and strong communication skills required.
- Other info: Collaborative team culture with opportunities for personal and professional growth.
The predicted salary is between 36000 - 47000 ÂŁ per year.
Hyper intelligence. Curious mindsets. Accelerated progress.
Regulatory Medical Writer
£36,000 – £49,000 plus benefits
Reports to: Medical Writing Manager
Directorate: Research & Innovation
Contract: Permanent
Hours: Full time 35 hours per week (flexible working requests considered, minimum 32 hours per week)
Location: Stratford, London (1-2 days a week in the office) * We’re happy to offer home‑based contracts through our flexible working policy.
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.
Recruitment process: Competency based interview followed by Medical Writing Task
At Cancer Research UK, we exist to beat cancer.
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.
As a Medical Writer you’ll be providing broad medical writing expertise for the production of clinical study reports, investigator brochures and other clinical/scientific reports for CDD’s early phase oncology trials. As well as acting as lead author on your assigned projects and performing quality control review of documents produced by other Medical Writers, you will be fully embedded within a multidisciplinary, cross‑functional project team along with other CDD departments. Collaboration is essential, as well as the ability to work strategically within an evolving environment.
Unfortunately, this role is not suitable for anyone who only has experience in medical writing for pharmacovigilance or medical devices or anyone who only has medical writing experience within science comms. You must come with strong knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results. This is a great opportunity for a current Regulatory Medical Writer looking to move into a more purpose‑driven environment or to gain valuable experience withing phase 1 oncology trials. Or you could be a Medical Writing Associate ready to take that next step.
What will I be doing?
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Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.
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Managing the preparation of clinical study reports by building consensus with the project teams on report requirements, responsibilities for delivery of data and production timelines, and participating in the preparation and review of summary clinical trial results and other disclosures as required.
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Managing the scheduling, preparation and updating of investigator brochure packages in use in CDD‑sponsored trials, ensuring review at least annually in line with current regulations.
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Liaising with the project team to complete project‑specific tasks including review of protocols, Trial Master Files, data (including expert reports), and analytical plans.
What are you looking for?
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Proven experience in medical / medical sciences writing. This should include significant experience in regulatory medical writing or a mix of experience in regulatory medical writing plus substantial relevant experience in a related role in clinical trials, pharmacovigilance or medical writing.
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Science graduate or equivalent experience of scientific writing.
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Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.
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Excellent proofreading skills and attention to detail.
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Confident communication skills and able to foster strong working relationships both internally and externally.
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Project Management skills.
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Experience within early phase oncology trials is desirable but not essential (Please do still apply even if you don’t have this).
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Experience within AI medical writing tools is beneficial.
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 recruitment@cancer.org.uk.
For more updates on our work and careers, follow us on: Linked In, Facebook, Instagram, X and YouTube.
Cancer Research UK is committed to safeguarding the wellbeing of its staff, volunteers, beneficiaries and other people who come into contact with the charity through all of its diverse range of activities. To review our safeguarding statement please visit Safeguarding at Cancer Research UK | Cancer Research UK
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 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.
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Regulatory Medical Writer employer: Cancer Research UK
Contact Detail:
Cancer Research UK Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Medical Writer
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for those interviews! Research the company, understand their mission, and be ready to discuss how your skills align with their goals. Practise common interview questions and think about how you can showcase your experience in regulatory medical writing.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email expressing your appreciation for the opportunity. It shows your enthusiasm and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! We love seeing applications come directly from candidates who are genuinely interested in joining us. Plus, it helps us keep track of your application more efficiently.
We think you need these skills to ace Regulatory Medical Writer
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your relevant experience in regulatory medical writing. We want to see how your skills align with the role, so don’t hold back on showcasing your expertise!
Showcase Your Attention to Detail: As a Regulatory Medical Writer, precision is key! Use your application to demonstrate your proofreading skills and attention to detail. A well-structured application will reflect your ability to produce high-quality documents.
Be Clear and Concise: When filling out the application form, keep your responses clear and to the point. We appreciate straightforward communication, so avoid jargon and focus on what makes you a great fit for the role.
Apply Early!: Don’t wait until the last minute to submit your application. We might close the vacancy early if we find the right candidate, so get your application in through our website as soon as possible to avoid disappointment!
How to prepare for a job interview at Cancer Research UK
✨Know Your Regulatory Stuff
Make sure you brush up on the regulatory requirements for clinical trial documents. Familiarise yourself with investigator brochures and clinical study reports, as these will likely come up in your interview. Being able to discuss these confidently will show that you’re serious about the role.
✨Showcase Your Writing Skills
Prepare a portfolio of your previous medical writing work, especially any regulatory documents you've authored. Be ready to discuss your writing process and how you ensure quality control. This is your chance to demonstrate your attention to detail and communication skills.
✨Emphasise Collaboration
Since this role involves working within multidisciplinary teams, be prepared to share examples of how you've successfully collaborated in the past. Highlight your project management skills and how you’ve built consensus with team members on report requirements and timelines.
✨Align with Their Values
Cancer Research UK values boldness, credibility, humanity, and teamwork. Think of examples from your experience that reflect these values and be ready to discuss them. Showing that you align with their mission to beat cancer will make a strong impression.
