Director of Regulatory Writing

JR United Kingdom; Stoke-on-Trent; On-site; GBP 60,000 - 100,000; Full time

Job summary

A leading company in medical communications is seeking experienced Directors of Regulatory Writing. The role focuses on leading complex projects, leveraging regulatory knowledge, and maintaining client relationships. Ideal candidates will have a background in pharmaceutical regulatory writing. Competitive benefits such as uncapped paid time off and flexible working arrangements are provided.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development opportunities

Employee assistance programme

Private healthcare

Headspace and MYNDUP mental health programmes

Cycle to work scheme

Season Ticket Loan

Flexible working arrangements

Qualifications

• Experience in pharmaceutical regulatory or medical writing.
• Strong understanding of regulatory documents and submission development.
• Leadership and client relationship management skills.

Responsibilities

• Lead complex regulatory writing projects.
• Guide team members and ensure effective medical writing.
• Maintain excellent client relationships.

Job description

Who are we?

Complete Regulatory is part of IPG Health Medical Communications, home to award-winning Med Comms agencies. We have 800 experts dedicated to combining science, creativity, and technology to deliver exceptional medical communications solutions for our clients.

What do we do?

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

The role

We seek experienced Directors of Regulatory Writing with a background in pharmaceutical regulatory or medical writing to join our team. You will leverage your knowledge of regulatory documents and submission development to lead complex projects and guide team members.

You will work as a trusted partner with clients, providing strategic leadership on a variety of projects and therapy areas, maintaining excellent client relationships, and ensuring effective medical writing for regulatory authorities.

What will you get in return?

This role offers an opportunity to develop your regulatory writing career within a supportive, reputable team. You will also benefit from our organisation's world-class services and flexible structure.

Benefits include:

• Flexible Time Off – uncapped paid time off
• Retail and gym discounts
• Training and development opportunities
• Employee assistance programme
• Private healthcare
• Headspace and MYNDUP mental health programmes
• Cycle to work scheme
• Season Ticket Loan
• Flexible working arrangements

To Apply or Contact Us

Apply via the link below. We celebrate diversity and encourage applicants from all backgrounds and abilities. Please let us know if any adjustments are needed during the application process.