Director of Regulatory Writing

JR United Kingdom; Luton; On-site; GBP 70,000 - 100,000; Full time

Job summary

A leading company in medical communications seeks a Director of Regulatory Writing in Luton. This role involves leading submissions and guiding teams in producing high-quality clinical documentation for the pharmaceutical industry. Join a reputable team offering flexible benefits, training opportunities, and a chance to enhance your regulatory writing experience.

Benefits

Flexible time off

Discounts and training

Healthcare and mental health programs

Cycle scheme

Season ticket loan

Flexible working arrangements

Qualifications

• Experience in pharmaceutical regulatory writing or medical writing agencies.
• Ability to lead complex submissions.
• Skill in serving as a trusted partner to clients.

Responsibilities

• Lead complex submissions and guide team members.
• Ensure effective medical writing for regulatory authorities.
• Provide writing support and consultancy services.

Skills

Strategic thinking

Leadership

Regulatory writing

Job description

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Director of Regulatory Writing, Luton, Bedfordshire

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Client:

Complete Regulatory | An IPG Health Company

Location:

Luton, Bedfordshire, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

6

Posted:

06.06.2025

Expiry Date:

21.07.2025

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Job Description:

Who are we?

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.

What do we do?

At Complete Regulatory, we provide class-leading writing support and consultancy services to the pharmaceutical industry, producing high-quality clinical documentation, including clinical study reports, protocols, clinical summaries, clinical overviews, regulatory responses, and other supporting documents across various therapy areas.

The role

We seek experienced Directors of Regulatory Writing with background in pharmaceutical regulatory writing or medical writing agencies. You will lead complex submissions, guide team members, and serve as a trusted partner to our clients, demonstrating strategic thinking and ensuring effective medical writing for regulatory authorities.

What will you get in return?

This role offers an excellent opportunity to build regulatory writing experience within a supportive and reputable team. Benefits include flexible time off, discounts, training, healthcare, mental health programs, cycle scheme, season ticket loan, and flexible working arrangements.

To Apply or Contact Us

Apply via the link below. IPG Health Medical Communications values diversity and encourages applicants of all backgrounds and abilities. Please inform us of any reasonable adjustments needed during the application process.