Senior Regulatory Writer

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

Job summary

A leading medical communications firm in Leeds is seeking a Senior Regulatory Writer to craft and review high-level regulatory documents for global submissions. The ideal candidate will develop high-quality regulatory documents and lead complex submissions while mentoring junior writers. With a degree in life sciences and experience in regulatory writing, you'll join a supportive and high-performing team. The position offers flexible time off, private healthcare, and various employee benefits.

Benefits

Flexible time off

Private healthcare

Life assurance

Pension

Mental health resources

Training and development

Retail and gym discounts

Qualifications

• Experience in pharma, med comms, or CRO is essential.
• Strong understanding of global submission standards.

Responsibilities

• Develop and deliver high-quality regulatory documents.
• Lead complex submissions including clinical overviews.
• Provide strategic consultancy to clients.
• Mentor junior writers.

Skills

Regulatory writing experience

Excellent 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!

Apply by clicking the link below.

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.