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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, collaborative culture, and significant growth opportunities.
- 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 collaborate with tech teams for real-world solutions.
The predicted salary is between 36000 - 60000 £ per year.
Location: United Kingdom (Remote / Hybrid)
Company: TriloDocs
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 Manchester 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 Manchester
✨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 recommend practising common interview questions with a friend to boost your confidence.
✨Tip Number 3
Showcase your expertise! Create a portfolio that highlights your best work, especially if you’ve tackled Module 2.7 or CSRs. We believe having tangible examples can really set you apart from other candidates.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Medical Writer in Manchester
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, so keep it engaging!
Showcase Your Technical Curiosity: Since we’re all about blending science with tech, let us know about any tools or platforms you’ve used in your writing process. If you’ve dabbled in document automation or worked with tech teams, make sure to mention that!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves!
How to prepare for a job interview at TriloDocs (part of Genactis Group)
✨Know Your Modules Inside Out
Make sure you’re well-versed in Module 2.7 and Module 2.5, as well as Clinical Study Reports. Brush up on the specifics and be ready to discuss your hands-on experience with these documents. This will show that you’re not just familiar with the content but can also apply it practically.
✨Show Off Your SME Skills
Since the role involves acting as a Subject Matter Expert, prepare examples of how you've guided teams in understanding regulatory writing workflows. Think about times when you’ve translated complex concepts into actionable insights—this will highlight your ability to bridge the gap between technical teams and medical writing.
✨Engage with Real-World Scenarios
Be ready to discuss real-world user needs and pain points in regulatory writing. Consider how you would approach client-facing calls and onboarding sessions. This will demonstrate your interpersonal skills and your ability to build trust-based relationships with clients.
✨Stay Current with Regulatory Guidelines
Familiarise yourself with the latest ICH, EMA, and FDA guidelines. Being able to reference current regulations during your interview will show that you’re proactive and committed to staying updated in the field, which is crucial for a Medical Writer at TriloDocs.
