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For Companies At a Glance
- Tasks: Write and review regulatory documents, ensuring clarity and compliance.
- Company: Join IPG Health Medical Communications, a leader in medical communications with a global impact.
- Benefits: Enjoy flexible time off, private healthcare, and wellness support among other perks.
- Why this job: Be part of a supportive team that values creativity and scientific precision.
- Qualifications: A degree in life sciences is preferred; prior regulatory writing experience is a plus.
- Other info: We celebrate diversity and encourage all backgrounds to apply.
The predicted salary is between 28800 - 48000 £ 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.
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.
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.
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: LinkedIn
Contact Detail:
LinkedIn Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Medical Writer
✨Tip Number 1
Familiarise yourself with the specific regulatory guidelines relevant to the pharmaceutical industry. Understanding the nuances of documents like Clinical Study Reports and Investigator’s Brochures will give you an edge in discussions during interviews.
✨Tip Number 2
Network with professionals already working in regulatory writing or medical communications. Engaging with them on platforms like LinkedIn can provide insights into the role and may even lead to referrals, which can significantly boost your chances.
✨Tip Number 3
Prepare to discuss your experience with managing multiple projects and timelines. Be ready to share specific examples of how you've successfully navigated challenges in previous roles, as this is a key aspect of the job.
✨Tip Number 4
Showcase your passion for science and precision during the interview. Be prepared to discuss recent developments in drug regulation or medical writing that excite you, as this demonstrates your genuine interest in the field.
We think you need these skills to ace Regulatory Medical Writer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Regulatory Medical Writer. Familiarise yourself with the types of documents you'll be writing and the skills needed to excel in this position.
Tailor Your CV: Customise your CV to highlight relevant experience in regulatory writing and any life sciences qualifications. Emphasise your ability to interpret complex scientific data and your previous work in medical communications or pharmaceutical settings.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for science and precision. Mention specific examples of your past work that align with the job description, such as writing Clinical Study Reports or collaborating with clients on regulatory submissions.
Proofread Your Application: Ensure that your application is free from errors. A well-written application reflects your attention to detail, which is crucial for a Regulatory Medical Writer. Consider asking a colleague or friend to review your documents before submission.
How to prepare for a job interview at LinkedIn
✨Showcase Your Writing Skills
As a Regulatory Medical Writer, your writing ability is crucial. Bring samples of your previous work to the interview, highlighting your experience with regulatory documents. Be prepared to discuss your writing process and how you ensure clarity and compliance.
✨Demonstrate Your Scientific Knowledge
Familiarise yourself with the latest trends in drug development and regulatory requirements. During the interview, be ready to discuss how you interpret complex scientific data and translate it into clear narratives for regulatory submissions.
✨Highlight Collaboration Experience
This role requires working closely with internal teams and clients. Share examples of past projects where you successfully collaborated with others, managed timelines, and met client expectations. Emphasise your ability to resolve issues proactively.
✨Prepare Questions About the Company
Show your interest in the company by preparing thoughtful questions about their work and culture. Ask about their approach to regulatory writing and how they support their writers' professional development. This demonstrates your enthusiasm and commitment to the role.
