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For Companies At a Glance
- Tasks: Write and review regulatory documents while collaborating with teams to ensure quality.
- Company: Join IPG Health Medical Communications, a leader in medical communications with over 800 experts.
- Benefits: Enjoy flexible time off, private healthcare, wellness support, and training opportunities.
- Why this job: Be part of a supportive team making complex science clear and impactful.
- Qualifications: A degree in life sciences is preferred; prior regulatory writing experience is a plus.
- Other info: Diversity is celebrated, and reasonable adjustments are available for applicants.
The predicted salary is between 28800 - 43200 £ 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.
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 specific regulatory guidelines and documentation requirements relevant to the pharmaceutical industry. Understanding these will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the medical communications field, especially those who work in regulatory writing. Engaging with them on platforms like LinkedIn can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences in regulatory writing during the interview. Be ready to share specific examples of how you've managed projects, collaborated with teams, and resolved issues in a fast-paced environment.
✨Tip Number 4
Showcase your passion for science and precision by staying updated on the latest trends and developments in drug regulation and medical writing. This knowledge can set you apart and demonstrate your enthusiasm for 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 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 experiences that demonstrate your writing skills and your understanding of drug development processes. Make it clear why you want to join IPG Health Medical Communications.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Ensure there are no grammatical errors or typos, as attention to detail is crucial in regulatory writing. A polished application reflects your professionalism and commitment.
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 to demonstrate your proficiency in crafting clear and compliant regulatory documents. Be prepared to discuss your writing process and how you ensure accuracy and adherence to guidelines.
✨Understand the Regulatory Landscape
Familiarise yourself with the latest regulations and guidelines relevant to the pharmaceutical industry. During the interview, be ready to discuss how these regulations impact your writing and the importance of compliance in regulatory submissions.
✨Highlight Collaborative Experiences
This role requires collaboration with various teams and clients. Share examples from your past experiences where you successfully worked with others to deliver high-quality documents on time. Emphasise your ability to manage multiple projects and communicate effectively.
✨Demonstrate Curiosity and Passion for Science
The ideal candidate is both clever and curious. Show your enthusiasm for science and regulatory writing by discussing recent developments in the field or specific areas of interest. This will help convey your passion and commitment to the role.
