Director of Regulatory Writing

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

Job summary

A leading company in medical communications seeks an experienced Director of Regulatory Writing to join their supportive team in the UK. This role involves guiding submissions, fostering client relationships, and using extensive regulatory knowledge to drive project success. Candidates should have a strong background in regulatory writing and project management, with flexibility and support throughout the application process.

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 options

Qualifications

• Experience in regulatory or medical writing within the pharmaceutical industry.
• Ability to lead complex submissions and guide team members.
• Strong strategic thinking and client relationship skills.

Responsibilities

• Lead complex submissions and ensure successful project delivery.
• Provide strategic insights and maintain excellent client relationships.
• Guide team members in regulatory writing practices.

Skills

Regulatory Writing

Project Management

Client Relationship Management

Job description

Who are we?

Complete Regulatory is part of IPG Health Medical Communications, home to celebrated and awarded 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 top-tier 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 supporting documents across various therapy areas.

The role

We seek experienced Directors of Regulatory Writing with background in regulatory or medical writing within the pharmaceutical industry or agencies. You will lead complex submissions, guide team members, and use your extensive knowledge of regulatory documents to ensure successful project delivery.

You will work as a trusted partner with clients, providing strategic insights and high-level leadership across diverse projects and therapy areas. Maintaining excellent client relationships and demonstrating strategic thinking will be key to your success in this role.

What will you get in return?

This role offers a great opportunity to enhance your regulatory writing career within a supportive, reputable team. You will join a larger organization offering world-class services and flexible working arrangements.

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 options

To Apply or Contact Us

Apply by clicking the link below. We celebrate diversity and welcome applicants from all backgrounds and abilities. Please let us know if you require any reasonable adjustments during the application process.