At a Glance
- Tasks: Write and edit clinical documents to support groundbreaking cancer research.
- Company: Join Cancer Research UK, a leader in charity-funded drug development.
- Benefits: Enjoy flexible working, competitive salary, and personal development opportunities.
- Other info: Collaborative environment with a focus on innovation and career growth.
- Why this job: Make a real difference in the fight against cancer while developing your writing skills.
- Qualifications: Experience in medical writing and a science background are essential.
The predicted salary is between 36000 - 49000 € per year.
£36,000 - £49,000 plus benefits
Reports to: Principal Medical Writer
Directorate: Research & Innovation
Contract: 24 months fixed term contract
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. 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.
Closing date: 3rd June 23:55pm
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 and Medical Writing task
Interview date: Approximately 12th / 15th June
Cancer Research UK are looking for a Regulatory Medical Writer to support our platform trial, DETERMINE. This exciting role sits within the CRUK Centre for Drug Development where our goal is to bring much needed new treatments to people with 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.
What will I be doing?
- Writing, editing, reviewing and quality control of documents for the timely production of clinical study reports and investigator brochures.
- 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.
- 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.
- 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?
- 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.
- Science graduate or equivalent experience of scientific writing.
- Good knowledge of regulatory requirements for clinical trial documents e.g. investigator brochures, clinical study reports and posting of clinical trial summary results.
- Excellent proofreading skills and attention to detail.
- Confident communication skills and able to foster strong working relationships both internally and externally.
- Project Management skills.
- Experience within early phase oncology trials is desirable but not essential (Please do still apply even if you don’t have this).
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. For more updates on our work and careers, follow us on LinkedIn, 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 us 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 Medical Writer in London employer: Cancer Research UK
At Cancer Research UK, we pride ourselves on being an exceptional employer, offering a supportive and inclusive work culture that prioritises employee wellbeing and professional growth. As a Regulatory Medical Writer, you will be part of a pioneering team dedicated to advancing cancer treatments, with access to generous benefits and flexible working arrangements that enhance work-life balance. Our commitment to collaboration and innovation ensures that every team member can contribute meaningfully to our mission of beating cancer while enjoying a fulfilling career path.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Medical Writer in London
✨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 your interview by practising common questions and scenarios related to regulatory medical writing. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 3
Showcase your skills! Bring along samples of your previous work or create a portfolio that highlights your best writing pieces. This will give you an edge and demonstrate your expertise during interviews.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, keep an eye on our careers page for new opportunities that match your skills and interests.
We think you need these skills to ace Regulatory Medical Writer in London
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Regulatory Medical Writer role. Highlight your relevant experience in medical writing and any specific projects that align with what we do at Cancer Research UK.
Showcase Your Skills:Don’t forget to emphasise your proofreading skills and attention to detail. We’re looking for someone who can manage documents meticulously, so give us examples of how you’ve done this in the past!
Be Clear and Concise:When filling out the online application form, keep your answers clear and to the point. We appreciate straightforward communication, especially when it comes to your work history and experiences.
Apply Through Our Website:Remember to apply through our website! It’s the best way for us to receive your application and ensures you’re considered fairly. Plus, you’ll find all the info you need about the role there.
How to prepare for a job interview at Cancer Research UK
✨Know Your Stuff
Make sure you brush up on your knowledge of regulatory medical writing and the specific requirements for clinical trial documents. Familiarise yourself with the types of reports you'll be working on, like clinical study reports and investigator brochures. This will show that you're not just interested in the role but also understand the nuances of the job.
✨Showcase Your Experience
Prepare to discuss your previous experience in medical writing or related fields. Be ready to share specific examples of projects you've worked on, especially those involving collaboration with cross-functional teams. Highlight any experience you have with early phase oncology trials, even if it's minimal, as it could set you apart from other candidates.
✨Ask Smart Questions
Interviews are a two-way street, so come prepared with thoughtful questions about the role and the team. Inquire about the current projects at Cancer Research UK and how the Regulatory Medical Writer fits into their mission. This shows your genuine interest in the organisation and helps you gauge if it's the right fit for you.
✨Emphasise Collaboration Skills
Since this role involves working closely with various project teams, be sure to highlight your ability to collaborate effectively. Share examples of how you've successfully worked in a team environment, managed project timelines, and built consensus on report requirements. This will demonstrate that you can thrive in a multidisciplinary setting.
