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- Tasks: Join us as a Regulatory Medical Writer, crafting essential clinical documents for the pharmaceutical industry.
- Company: Complete Regulatory is part of IPG Health, renowned for exceptional medical communications solutions.
- Benefits: Enjoy flexible time off, retail discounts, private healthcare, and wellness programmes.
- Why this job: This role offers a chance to grow in a supportive team while making a real-world impact.
- Qualifications: Ideal candidates are life-science graduates with writing experience; PhD preferred but not mandatory.
- Other info: We celebrate diversity and encourage all backgrounds to apply, ensuring an inclusive hiring process.
The predicted salary is between 30000 - 50000 £ per year.
Complete Regulatory is part of IPG Health Medical Communications, home to the world’s most awarded and celebrated Med Comms agencies. With over 800 dedicated experts, we combine science, creativity, and technology to craft exceptional medical communications solutions for leading pharmaceutical companies worldwide.
What We Do
We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Our work spans a wide range of high-quality clinical and regulatory documents, including:
- Clinical Study Reports (CSRs)
- Protocols and Amendments
- Clinical Summaries and Overviews (for CTD Modules 2.5 & 2.7)
- Regulatory responses to health authorities
- Investigator’s Brochures and other supporting documentation
We work across a variety of therapy areas, partnering with clients at all stages of drug development and submission.
The Role: Regulatory Writer
We’re looking for experienced Regulatory Writers who are both clever and curious, with a passion for science and precision. You’ll play a key role in interpreting and communicating complex scientific data clearly and accurately for regulatory submissions worldwide.
Key Responsibilities
- Write, edit, and review regulatory documents in accordance with guidelines and client requirements
- Analyze and interpret scientific data to develop coherent and compliant narratives
- Collaborate with internal teams and clients to ensure high-quality, timely deliverables
- Manage multiple projects, timelines, and client expectations effectively
- Proactively resolve project-related issues and contribute to continuous improvement
What You’ll Bring
- A degree in a life sciences discipline (PhD or research experience preferred, but not essential)
- Prior regulatory writing experience in a medical communications company, CRO or Pharma
- A solid understanding of drug development and regulatory documentation requirements
- Excellent writing, communication, and organizational skills
- Ability to work both independently and collaboratively in a fast-paced environment
What You’ll Get in Return
This is an opportunity to advance your career in regulatory writing within a highly specialised, supportive, and reputable team, while benefiting from the broader offerings of IPG Health Medical Communications.
We offer a competitive rewards package, including:
- Flexible Time Off – uncapped paid leave
- Private healthcare and life assurance
- Pension scheme
- Mental health & wellness support – including Headspace and MYNDUP
- Training & development opportunities
- Retail and gym discounts
- Cycle to work scheme
- Season ticket loan
- Employee Assistance Programme
- Long Service Awards
- Flexible/hybrid working options
If you’re a detail-oriented writer who thrives on making complex science clear, and you\’re looking for a fresh challenge in a collaborative and forward-thinking environment, we’d love to hear from you.
To Apply or Contact Us
Apply by clicking the link below.
IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creating exceptional medical communications for our clients. Our people are the beating heart of our organisation, and through the positive culture we champion, our teams create communications that not only have a positive impact for our clients, but also impact on the world around us.
We celebrate diversity and encourage applicants from all whatever their background and/or disability. We want you to have every opportunity to shine and show us your talents, so please reach out and let us know if there are any reasonable adjustments we can make to ensure our assessment process works for you.
Regulatory Medical Writer employer: Complete Regulatory | An IPG Health Company
Contact Detail:
Complete Regulatory | An IPG Health Company Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Medical Writer
✨Tip Number 1
Reach out directly to the job poster on LinkedIn. A personalised message expressing your interest in the Regulatory Medical Writer position can help you stand out and make a memorable impression.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in the pharmaceutical industry. Being knowledgeable about current practices will not only boost your confidence but also demonstrate your commitment to the field during any discussions.
✨Tip Number 3
Network with professionals already working in regulatory writing or related fields. Attend industry events or webinars to connect with potential colleagues and gain insights that could be beneficial during interviews.
✨Tip Number 4
Prepare for potential interview questions by practising how you would discuss your experience with complex scientific data and project management. Being articulate about your skills will help you convey your suitability for the role effectively.
We think you need these skills to ace Regulatory Medical Writer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant writing experience in the pharmaceutical industry. Emphasise any specific projects or documents you've worked on that align with the role of a Regulatory Medical Writer.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical communications and your understanding of regulatory writing. Mention how your skills and experiences make you a great fit for Complete Regulatory.
Highlight Communication Skills: In your application, provide examples of how you've effectively communicated complex scientific data in previous roles. This is crucial for the analysis and critique required in regulatory submissions.
Showcase Project Management Experience: Detail any project management experience you have, especially in managing competing projects. This will demonstrate your ability to handle the demands of the role efficiently.
How to prepare for a job interview at Complete Regulatory | An IPG Health Company
✨Showcase Your Writing Skills
As a Regulatory Medical Writer, your writing ability is crucial. Bring samples of your previous work that demonstrate your proficiency in creating clinical documentation. Be prepared to discuss your writing process and how you ensure accuracy and clarity in complex scientific data.
✨Understand the Pharmaceutical Landscape
Familiarise yourself with the pharmaceutical industry and current regulatory requirements. During the interview, reference specific regulations or guidelines relevant to the role, showing that you are knowledgeable and engaged with the field.
✨Demonstrate Project Management Experience
Highlight your project management skills by discussing how you've successfully managed competing projects in the past. Provide examples of how you prioritised tasks, met deadlines, and resolved any issues that arose during the writing process.
✨Prepare Questions for the Interviewers
Engage with your interviewers by preparing thoughtful questions about the company culture, team dynamics, and expectations for the role. This shows your genuine interest in the position and helps you assess if the company is the right fit for you.
