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- Tasks: Shape the future of regulatory writing technology and support innovative product development.
- Company: Join TriloDocs, a fast-growing tech company revolutionising medical writing.
- Benefits: Flexible remote/hybrid work, growth opportunities, and a collaborative culture.
- Why this job: Leverage your expertise to make a strategic impact in a dynamic environment.
- Qualifications: 2-5 years of regulatory medical writing experience and strong communication skills.
- Other info: Engage directly with clients and contribute to cutting-edge solutions.
The predicted salary is between 36000 - 60000 £ per year.
Location: United Kingdom (Remote / Hybrid)
About TriloDocs
TriloDocs is a fast-growing tech company transforming how clinical and regulatory documents are created. We combine scientific expertise with powerful automation tools to help biotech and pharma organizations accelerate high-quality submissions. As we expand, we're looking for a Medical Writing Specialist who is excited about both regulatory science and modern technology.
Role Overview
We are seeking a UK-based Medical Writing Specialist with 2–5 years of hands-on regulatory medical writing experience, particularly with Module 2.7 (Clinical Overview) and Module 2.5 (Clinical Summary) and/or Clinical Study Reports (CSRs). Unlike traditional writing roles, this position focuses on acting as a Subject Matter Expert (SME) to support our internal technical and product teams. You’ll help us understand regulatory writing workflows, interpret industry best practices, and ensure our technology aligns with how medical writers actually think and work. You will also engage directly with clients on early sales, onboarding, and support calls—helping translate medical writing needs into product solutions and building strong, trust-based relationships.
Key Responsibilities
- Serve as an internal SME on regulatory medical writing, including CSRs and Module 2 summaries.
- Guide product and technical teams in understanding regulatory writing workflows, pain points, and real-world user needs.
- Participate in client-facing calls, including early sales conversations and support/onboarding sessions.
- Translate medical writing requirements into actionable insights for our tech and product teams.
- Contribute to the development of templates, workflows, user training, and product improvements.
- Stay current with ICH, EMA, FDA and other relevant regulatory guidelines.
Required Qualifications
- 2–5 years of regulatory medical writing experience (biotech, pharma or CRO).
- Hands-on writing experience of Module 2.7, Module 2.5, and/or CSR and full-cycle understanding of delivery structure and requirements.
- Based in the United Kingdom and eligible to work there.
- Strong technical curiosity—comfortable learning new tools and collaborating with engineers and product managers.
- Excellent interpersonal and communication skills; enjoys engaging with clients.
- Ability to explain complex regulatory concepts clearly and succinctly.
Nice-to-Have
- Experience working with or supporting technology teams.
- Exposure to document automation or regulatory writing platforms.
- Startup or fast-paced environment experience.
Why Join TriloDocs?
- Help shape the next generation of regulatory writing technology.
- Use your medical writing expertise in a new, forward-looking way—less writing, more strategic influence.
- Work in a collaborative, innovative culture with significant growth opportunities.
- Flexible, UK-based remote/hybrid working options.
Medical Writer in Leeds employer: TriloDocs (part of Genactis Group)
Contact Detail:
TriloDocs (part of Genactis Group) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer in Leeds
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical writing field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory guidelines and recent trends in medical writing. We want you to shine as the Subject Matter Expert they’re looking for!
✨Tip Number 3
Don’t just apply—engage! When you submit your application through our website, follow up with a friendly email expressing your enthusiasm for the role. It shows initiative and keeps you on their radar.
✨Tip Number 4
Showcase your tech-savviness! Be ready to discuss how you’ve used technology in your previous roles. We know TriloDocs values innovation, so highlight any experience with document automation or regulatory writing platforms.
We think you need these skills to ace Medical Writer in Leeds
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your regulatory medical writing experience, especially with Module 2.7 and Module 2.5. We want to see how your skills align with our needs, so don’t be shy about showcasing relevant projects!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about the role and how your background makes you a perfect fit. Remember, we love seeing your personality come through!
Showcase Your Communication Skills: Since this role involves engaging with clients and internal teams, highlight any experiences where you’ve successfully communicated complex ideas. We’re looking for clear and concise communicators who can bridge the gap between tech and writing.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at TriloDocs (part of Genactis Group)
✨Know Your Modules
Make sure you brush up on Module 2.7 and Module 2.5, as well as Clinical Study Reports. Be ready to discuss your hands-on experience with these documents and how they fit into the regulatory writing process. This will show that you’re not just familiar with the content but also understand its significance in the industry.
✨Show Your Technical Curiosity
TriloDocs values a strong technical curiosity, so be prepared to talk about any tools or technologies you've used in your previous roles. If you have experience with document automation or regulatory writing platforms, highlight that! It’s all about demonstrating how you can bridge the gap between medical writing and technology.
✨Engage with Real-World Scenarios
During the interview, think of examples where you’ve had to translate complex regulatory concepts into actionable insights. Discuss how you’ve interacted with clients or internal teams to solve problems. This will showcase your ability to communicate effectively and work collaboratively, which is key for the role.
✨Stay Updated on Regulations
Make sure you’re up-to-date with the latest ICH, EMA, and FDA guidelines. Being knowledgeable about current regulations will not only help you answer questions confidently but also demonstrate your commitment to staying informed in a fast-paced environment. Bring up any recent changes you’ve followed and how they might impact your work.
