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- Tasks: Write high-quality regulatory documents for the pharmaceutical industry and support clients with strategic insights.
- Company: Join Complete Regulatory, part of IPG Health, a leader in medical communications with a creative and scientific edge.
- Benefits: Enjoy flexible time off, retail discounts, private healthcare, and a supportive work environment.
- Why this job: Advance your career in a reputable team while making a positive impact on healthcare communications.
- Qualifications: 3+ years as a regulatory writer; life-science degree preferred, PhD or research experience is a plus.
- Other info: We celebrate diversity and encourage applicants from all backgrounds to apply.
The predicted salary is between 43200 - 72000 £ per year.
Complete Regulatory is part of IPG Health Medical Communications, home to the world’s most celebrated and awarded Med Comms agencies. We are 800 experts obsessed with combining science, creativity, and technology to create exceptional medical communications solutions for our clients.
We provide class-leading writing support and consultancy services to the pharmaceutical industry, producing a wide range of high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory responses and other supporting documents, across a variety of therapy areas.
We are looking to recruit Senior Regulatory Writers with at least 3 years' experience as a regulatory writer within the pharmaceutical industry and/or a medical writing agency. Applicants should be life-science graduates, ideally with a PhD or other research experience, although this is not mandatory. You will use your thorough knowledge of FDA, EMA and ICH guidelines to write a wide range of regulatory documents; these will include strategic requirements, such as clinical overviews, higher-level summaries and briefing documents. You will also help to maintain our excellent client relationships, which will allow you to consult with the client and demonstrate your high-level strategic thinking, based on extensive past experience, to ensure effective medical writing for regulatory authorities. You will be a highly valued member of the Regulatory Writing team and will have the opportunity to advance your skills while helping less experienced team members to achieve their potential, by providing coaching and insight.
This position will benefit anyone looking to build on their experience in regulatory writing, while working within a highly specialised, supportive and reputable team. In addition, you will become part of a larger organisation, which offers a range of world-class services and a flexible organisational structure. As well as a fresh challenge in your career, long term career choices and development, you will be rewarded with:
- Flexible Time Off – uncapped paid time off
- Retail and gym discounts
- Great training and development
- Life assurance
- Pension
- Employee assistance programme
- Private healthcare
- Headspace and MYNDUP - a mental health wellness programme
- Cycle to work scheme
- Long Service Award
- Season Ticket Loan
- Flexible working
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 backgrounds and/or disabilities. 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.
Contact Detail:
IPG Health Medical Communications Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Writer
✨Tip Number 1
Familiarise yourself with the latest FDA, EMA, and ICH guidelines. Being well-versed in these regulations will not only boost your confidence but also demonstrate your expertise during any discussions or interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry and medical writing community. Attend relevant conferences or webinars to connect with potential colleagues and learn about the latest trends in regulatory writing.
✨Tip Number 3
Prepare to discuss your past experiences in detail, especially those that highlight your strategic thinking and client relationship management. Be ready to share specific examples of how you've successfully navigated complex regulatory writing projects.
✨Tip Number 4
Showcase your ability to mentor and coach others in your field. Highlight any previous experience where you’ve helped less experienced writers develop their skills, as this aligns with the collaborative culture at Complete Regulatory.
We think you need these skills to ace Senior Regulatory Writer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Senior Regulatory Writer. Familiarise yourself with the types of documents you'll be expected to produce and the regulatory guidelines involved.
Tailor Your CV: Highlight your relevant experience in regulatory writing within the pharmaceutical industry or medical writing agencies. Emphasise any specific projects or documents you've worked on that align with the job description.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for medical communications and your understanding of FDA, EMA, and ICH guidelines. Mention how your background and skills make you a perfect fit for the role and how you can contribute to maintaining excellent client relationships.
Proofread Your Application: Ensure that your application is free from errors and clearly communicates your qualifications. A well-written application reflects your attention to detail, which is crucial for a regulatory writer.
How to prepare for a job interview at IPG Health Medical Communications
✨Know Your Guidelines
Familiarise yourself with FDA, EMA, and ICH guidelines before the interview. Being able to discuss these regulations confidently will demonstrate your expertise and understanding of the regulatory landscape.
✨Showcase Your Experience
Prepare specific examples from your past work as a regulatory writer. Highlight projects where you successfully produced clinical documentation and how your contributions positively impacted client relationships.
✨Demonstrate Strategic Thinking
Be ready to discuss how you approach writing strategic documents like clinical overviews and briefing documents. Illustrate your thought process and how you ensure that your writing meets both client needs and regulatory requirements.
✨Emphasise Team Collaboration
Since you'll be part of a team, share experiences where you've coached or supported less experienced colleagues. This shows your ability to work collaboratively and contribute to the development of others in the field.
