Director of Regulatory Writing

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

Job summary

A leading medical communications company seeks a Director of Regulatory Writing in Basingstoke. This role involves leading regulatory submissions, mentoring team members, and strategizing documentation processes. Candidates should have experience in pharmaceutical writing, with a strong focus on delivering effective solutions in a collaborative environment.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development

Employee assistance program

Private healthcare

Headspace and MYNDUP mental health programs

Cycle to work scheme

Season Ticket Loan

Flexible working

Qualifications

• Experience in pharmaceutical or medical writing agencies.
• Proven track record of leading complex submissions.
• Ability to guide team members effectively.

Responsibilities

• Lead complex regulatory submissions for the pharmaceutical industry.
• Guide and mentor team members in writing processes.
• Serve as a trusted partner to clients in regulatory documentation.

Skills

Strategic Thinking

Leadership

Regulatory Documentation

Job description

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Director of Regulatory Writing, Basingstoke

Client: Complete Regulatory | An IPG Health Company

Location:

Job Category:

Other

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EU work permit required:

Yes

Job Views:

3

Posted:

31.05.2025

Expiry Date:

15.07.2025

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.

What do we do?

We provide leading writing support and consultancy services to the pharmaceutical industry, producing 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. You will lead complex submissions, guide team members, and serve as a trusted partner to our clients, demonstrating strategic thinking to ensure effective regulatory documentation.

What will you get in return?

This role offers a great opportunity for growth within a supportive, reputable team. Benefits include:

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

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.