Director of Regulatory Writing

JR United Kingdom; Chelmsford; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading company in medical communications is seeking a Director of Regulatory Writing to enhance their team in Chelmsford. This role involves leading regulatory submissions and maintaining strong client relationships. The ideal candidate will possess extensive knowledge in medical writing and a background in the pharmaceutical industry, offering a chance to work in a supportive environment with a reputable organization.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development opportunities

Employee assistance program

Private healthcare

Wellness programs (Headspace, MYNDUP)

Cycle to work scheme

Season Ticket Loan

Flexible working options

Qualifications

• Prior experience in regulatory or medical writing within the pharmaceutical industry or agencies is essential.
• Extensive knowledge of regulatory documents required.
• Experience in leading complex submissions.

Responsibilities

• Lead complex regulatory submissions and guide team members.
• Work closely with clients to provide strategic leadership and maintain strong relationships.
• Ensure effective medical writing for regulatory authorities.

Skills

Leadership

Regulatory writing

Medical writing

Client relations

Education

Bachelor's degree in Life Sciences or related field

Job description

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Director of Regulatory Writing, Chelmsford

Client:

Complete Regulatory | An IPG Health Company

Location:

Chelmsford

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 the world’s most celebrated and awarded Med Comms agencies. We are 800 experts obsessed with combining science, creativity, and technology to create 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. We produce high-quality clinical documentation, including 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 prior experience 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 closely with clients, providing strategic leadership, maintaining strong relationships, and ensuring effective medical writing for regulatory authorities.

What will you get in return?

This role offers an excellent opportunity to enhance your regulatory writing experience within a supportive, reputable team. You will be part of 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 program
• Private healthcare
• Wellness programs (Headspace, MYNDUP)
• Cycle to work scheme
• Season Ticket Loan
• Flexible working options

To Apply or Contact Us

Apply via the link below.

IPG Health Medical Communications values diversity and encourages applicants from all backgrounds and abilities. Please inform us of any reasonable adjustments needed during the application process.