Senior Regulatory Writer

Complete Regulatory | An IPG Health Company; Birmingham; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading regulatory affairs firm in Birmingham seeks a Senior Regulatory Writer to craft high-level regulatory documents for global submissions. This role involves leading complex submissions and mentoring junior writers. Ideal candidates should have a relevant degree, regulatory writing experience in the pharmaceutical sector, and strong skills in scientific writing and project management. The position offers flexible time off and private healthcare, among other benefits.

Benefits

Flexible time off

Private healthcare

Pension

Mental health resources

Training and development

Gym discounts

Qualifications

• Minimum experience in regulatory writing within pharma, med comms, or a CRO.
• Strong understanding of global submission standards.
• Collaborative and quality-driven mindset.

Responsibilities

• Develop and deliver high-quality regulatory documents aligned with global guidelines.
• Lead complex submissions, including clinical overviews and briefing packages.
• Provide strategic consultancy to clients.
• Mentor junior writers.

Skills

Regulatory writing experience

Scientific writing

Project management

Interpersonal skills

Education

Degree in life sciences

PhD (advantageous)

Job description

Join Complete Regulatory , part of IPG Health Medical Communications , a global network of award-winning med comms agencies with 500+ experts. We combine science, creativity, and technology to deliver top-tier medical communications solutions.

The Role

We’re looking for Senior Regulatory Writers to craft and review high-level regulatory documents for global submissions. This is your chance to work on strategic clinical overviews, summaries, and briefing packages, while guiding junior writers and advising clients.

What You’ll Do

• Develop and deliver high-quality regulatory documents aligned with global guidelines
• Lead complex submissions, including clinical overviews and briefing packages
• Provide strategic consultancy to clients
• Mentor junior writers and strengthen team expertise

What You’ll Bring

• Degree in life sciences (PhD advantageous)
• Regulatory writing experience in pharma, med comms, or a CRO
• Strong understanding of global submission standards
• Excellent scientific writing, project management, and interpersonal skills
• Collaborative, flexible, and quality-driven mindset

Perks & Benefits

• Flexible time off
• Private healthcare, life assurance, pension
• Mental health resources (Headspace, MYNDUP)
• Training, development, and career growth
• Retail and gym discounts, cycle-to-work scheme, long service awards

If you’re ready to take your regulatory writing career to the next level with a supportive, high-performing team, apply now !

To Apply or Contact Us

Apply by clicking the link below.

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.