Director of Regulatory Writing

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

Job summary

JR United Kingdom is seeking an experienced Director of Regulatory Writing to enhance its team in Swindon. This key position entails leading regulatory submissions and providing strategic guidance within a renowned company known for its exceptional medical communications. The role also offers significant career development opportunities along with flexible working arrangements and various beneficial perks.

Benefits

Flexible time off

Discounts

Training

Healthcare

Mental health programmes

Cycle scheme

Season ticket loan

Flexible working arrangements

Qualifications

• Experience in pharmaceutical or medical writing agencies.
• Proven track record of leading submissions.
• Exceptional communication and any relevant certifications.

Responsibilities

• Lead complex submissions to regulatory authorities.
• Provide strategic guidance to clients.
• Mentor team members on writing standards.

Skills

Regulatory writing

Strategic guidance

Mentorship

Job description

Director of Regulatory Writing, Swindon, Wiltshire

Client: Complete Regulatory | An IPG Health Company

Location: Swindon, Wiltshire, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Views: 19

Posted: 27.06.2025

Expiry Date: 11.08.2025

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 other supporting documents across various therapy areas.

The role

We seek experienced Directors of Regulatory Writing with a background in pharmaceutical or medical writing agencies to lead complex submissions and mentor team members. You will work closely with clients to provide strategic guidance and ensure high-quality medical writing for regulatory authorities.

What will you get in return?

This role offers an excellent opportunity for career development within a supportive, reputable team. Benefits include flexible time off, discounts, training, healthcare, mental health programmes, cycle scheme, season ticket loan, and flexible working arrangements.

To Apply or Contact Us

Apply via the link below. We celebrate diversity and encourage applicants from all backgrounds. Please inform us of any reasonable adjustments needed during the application process.