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- Tasks: Join us as a Regulatory Medical Writer, crafting high-quality 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 a supportive work environment.
- Why this job: This role offers a chance to grow in regulatory writing while making a real-world impact.
- Qualifications: Life-science graduates with writing experience in pharma or agencies are preferred; PhD not mandatory.
- Other info: We celebrate diversity and encourage all backgrounds to apply, ensuring an inclusive assessment process.
The predicted salary is between 36000 - 60000 £ 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 Regulatory Writers with clever and curious minds. Relevant writing experience gained within the pharmaceutical industry or an agency is essential. Applicants should be life-science graduates, ideally with a PhD or other research experience, although this is not mandatory.
Your excellent communication and organisational skills will be required in the analysis, interpretation and critique of complex scientific data, which are used in regulatory submissions to national authorities throughout the world. You will also use your project management skills to efficiently manage competing projects as well as your client management skills to resolve any issues in a timely manner.
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 Regulatory Medical Writer
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and standards in the pharmaceutical industry. This knowledge will not only help you understand the role better but also demonstrate your commitment and expertise during discussions.
✨Tip Number 2
Network with professionals in the medical writing field, especially those who work in regulatory writing. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the sector.
✨Tip Number 3
Prepare to discuss specific examples of your previous writing experience, particularly any that involved complex scientific data. Being able to articulate how you've successfully managed projects or resolved issues will set you apart from other candidates.
✨Tip Number 4
Showcase your organisational and project management skills by discussing how you prioritise tasks and manage competing deadlines. This is crucial for a Regulatory Medical Writer, so be ready to provide concrete examples of your strategies.
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 or an agency. Emphasise any life-science qualifications, especially if you have a PhD or research experience.
Craft a Compelling Cover Letter: Write a cover letter that showcases your communication and organisational skills. Discuss your ability to analyse complex scientific data and how your project management skills can benefit the team.
Showcase Your Passion for Medical Writing: In your application, express your enthusiasm for regulatory writing and how it aligns with your career goals. Mention any specific areas of interest within medical communications that excite you.
Proofread and Edit: Before submitting your application, thoroughly proofread all documents. Ensure there are no grammatical errors or typos, as attention to detail is crucial in regulatory writing.
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 or be prepared to discuss specific projects where you demonstrated your writing skills in the pharmaceutical industry.
✨Understand Regulatory Requirements
Familiarise yourself with the regulatory landscape relevant to the role. Being able to discuss key regulations and guidelines will show that you are knowledgeable and serious about the position.
✨Demonstrate Project Management Experience
Highlight any experience you have in managing multiple projects simultaneously. Discuss how you prioritised tasks and resolved issues, as this is essential for the role.
✨Prepare for Technical Questions
Expect questions that assess your understanding of complex scientific data. Brush up on your knowledge of clinical documentation and be ready to explain how you would approach analysing and interpreting such data.
