Director of Regulatory Writing

JR United Kingdom; Nottingham; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading medical communications company seeks a Director of Regulatory Writing in Nottingham. This role involves leading projects and mentoring writers while ensuring high-quality documentation for regulatory submissions. Join a reputable team with excellent benefits, including uncapped paid time off and flexible working arrangements.

Benefits

Uncapped paid time off

Retail and gym discounts

Training and development opportunities

Employee assistance program

Private healthcare

Mental health wellness programs

Cycle to work scheme

Season Ticket Loan

Flexible working arrangements

Qualifications

• Experienced in regulatory documentation and submission development.
• Ability to mentor team members in regulatory writing.
• Background in pharmaceutical or medical writing agencies.

Responsibilities

• Lead complex regulatory writing projects.
• Provide strategic guidance to clients.
• Maintain high standards of medical writing.

Skills

Regulatory writing

Project leadership

Client relationship management

Job description

Job Title: Director of Regulatory Writing, Nottingham

Client:

Complete Regulatory | An IPG Health Company

Location:

Nottingham, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

6

Posted:

06.06.2025

Expiry Date:

21.07.2025

Job Description:

Who are we?

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

What do we do?

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 more across various therapy areas.

The role

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

You will work closely with clients, providing strategic guidance and ensuring high standards in medical writing for regulatory authorities, maintaining strong client relationships.

What will you get in return?

This role offers a chance to enhance your regulatory writing expertise within a supportive, reputable team. Benefits include:

• Uncapped paid time off
• Retail and gym discounts
• Training and development opportunities
• Employee assistance program
• Private healthcare
• Mental health wellness programs
• Cycle to work scheme
• Season Ticket Loan
• Flexible working arrangements

How to apply

Click the link below to submit your application.

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