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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: Ideal candidates are life-science graduates with regulatory writing experience; PhD preferred but not mandatory.
- 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, which comprises 800 experts obsessed with combining science, creativity, and technology to create exceptional medical communications solutions for our clients.
At Complete Regulatory, 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 previous 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
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:
Complete Regulatory | An IPG Health Company 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 commitment to the role during any discussions or interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical and medical writing fields. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends, which can give you an edge when discussing your experience.
✨Tip Number 3
Prepare to discuss specific examples of your past regulatory writing experiences. Think about challenges you've faced and how you overcame them, as this will showcase your problem-solving skills and strategic thinking during interviews.
✨Tip Number 4
Showcase your ability to mentor and support less experienced team members. Highlight any coaching or training experiences you've had, as this aligns with the role's emphasis on teamwork and development within the Regulatory Writing team.
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: Craft your CV to highlight relevant experience in regulatory writing and any specific knowledge of FDA, EMA, and ICH guidelines. Emphasise your life-science background and any research experience that aligns with the job description.
Write a Compelling Cover Letter: Your cover letter should reflect your passion for medical communications and your understanding of the pharmaceutical industry. Use specific examples from your past experience to demonstrate your strategic thinking and ability to maintain client relationships.
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 role in regulatory writing. Consider asking a colleague or friend to review your documents before submission.
How to prepare for a job interview at Complete Regulatory | An IPG Health Company
✨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 to discuss specific examples from your past roles as a regulatory writer. Highlight your contributions to clinical documentation and how you maintained client relationships, as this will show your practical experience in the field.
✨Emphasise Team Collaboration
Since the role involves coaching less experienced team members, be ready to talk about your teamwork and mentoring experiences. Share how you've helped others grow and how you value collaboration in achieving high-quality outcomes.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's projects, team dynamics, and future goals. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.
