Regulatory Medical Writer

Regulatory Medical Writer

Stratford-upon-Avon Full-Time 36000 - 47000 Β£ / year (est.) Home office (partial)
Go Premium
C

At a Glance

  • Tasks: Write and edit clinical documents to support cancer research projects.
  • Company: Join Cancer Research UK, a leading charity making a difference in oncology.
  • Benefits: Generous benefits package, flexible working, and personal development opportunities.
  • Why this job: Make an impact in cancer research while developing your writing skills.
  • Qualifications: Experience in medical writing and a science degree required.
  • Other info: Inclusive culture that values diversity and supports your wellbeing.

The predicted salary is between 36000 - 47000 Β£ per year.

Overview

Regulatory Medical Writer role at Cancer Research UK (CRUK)

Location: Stratford, London (1-2 days a week in the office). Home-based contracts available.

Salary: Β£36,000 – Β£47,000 plus benefits

Reports to: Medical Writing Manager or Principal Medical Writer

Directorate: Research & Innovation

Contract: 2 contracts – 1x 15 months fixed term and 1x 2 years fixed term

Hours: Full time 35 hours per week (flexible working requests considered, minimum 32 hours per week)

Closing date: 5 October 2025 23:55

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.
  • 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)
  • Experience within AI medical writing tools is beneficial.

Our organisation values

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

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: LinkedIn, 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. Please 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.

Seniority level

  • Entry level

Employment type

  • Full-time

Job function

  • Marketing, Public Relations, and Writing/Editing

Industries

  • Non-profit Organizations

#J-18808-Ljbffr

Regulatory Medical Writer employer: Cancer Research UK (CRUK)

Cancer Research UK is an exceptional employer that prioritises employee wellbeing and professional growth, offering a flexible working environment in Stratford, London. With a generous benefits package and a commitment to inclusivity, CRUK fosters a collaborative culture where employees can thrive while contributing to impactful research in the fight against cancer.
C

Contact Detail:

Cancer Research UK (CRUK) 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 professionals in the medical writing field on LinkedIn or at industry events. A friendly chat can open doors and give you insights that job descriptions just can't.

✨Tip Number 2

Prepare for your interview by brushing up on regulatory requirements and recent developments in clinical trials. Show us you’re not just a candidate, but someone who’s genuinely passionate about making an impact in oncology.

✨Tip Number 3

Practice your communication skills! Whether it’s explaining complex medical concepts or discussing your previous experiences, being clear and confident will help you stand out during interviews.

✨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, we love seeing candidates who take the initiative to engage with us directly.

We think you need these skills to ace Regulatory Medical Writer

Regulatory Medical Writing
Clinical Study Reports
Investigator Brochures
Proofreading Skills
Attention to Detail
Communication Skills
Project Management
Knowledge of Regulatory Requirements
Experience in Clinical Trials
Liaising with Project Teams
Analytical Skills
Experience with AI Medical Writing Tools
Ability to Build Consensus
Flexibility in Working Hours

Some tips for your application 🫑

Tailor Your Application: Make sure to customise your application to highlight your relevant experience in regulatory medical writing. We want to see how your background aligns with the role, so don’t hold back on showcasing your skills!

Show Off Your Attention to Detail: As a Regulatory Medical Writer, attention to detail is key. When you’re writing your application, double-check for any typos or errors. We appreciate candidates who take pride in their work and can demonstrate excellent proofreading skills.

Be Clear and Concise: Keep your application straightforward and to the point. We love clarity, so make sure your writing is easy to follow. Use bullet points where necessary to break down your experience and skills effectively.

Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered fairly in our anonymised shortlisting process. We can’t wait to hear from you!

How to prepare for a job interview at Cancer Research UK (CRUK)

✨Know Your Stuff

Make sure you brush up on your knowledge of regulatory requirements for clinical trial documents. Familiarise yourself with investigator brochures and clinical study reports, as these will likely come up in conversation. Being able to discuss these confidently will show that you're serious about the role.

✨Showcase Your Experience

Prepare specific examples from your past work that highlight your experience in medical writing and project management. Think about times when you successfully managed timelines or collaborated with project teams. This will help demonstrate your ability to handle the responsibilities of the role.

✨Ask Smart Questions

Come prepared with thoughtful questions about the team dynamics, ongoing projects, or the use of AI tools in medical writing. This not only shows your interest in the position but also gives you a chance to assess if the company culture aligns with your values.

✨Be Yourself

Cancer Research UK values inclusivity and collaboration, so don’t be afraid to let your personality shine through. Share your passion for medical writing and how you can contribute to their mission. Authenticity can make a lasting impression!

Regulatory Medical Writer
Cancer Research UK (CRUK)
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

C
  • Regulatory Medical Writer

    Stratford-upon-Avon
    Full-Time
    36000 - 47000 Β£ / year (est.)

    Application deadline: 2027-10-09

  • C

    Cancer Research UK (CRUK)

Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>