Regulatory Medical Writer

JR United Kingdom; Wolverhampton; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading health communications agency is seeking a Regulatory Medical Writer to join their team in Wolverhampton. The ideal candidate will have experience in scientific writing, particularly in the pharmaceutical industry, and will be adept at managing complex projects. This role offers flexible working conditions and a range of benefits aimed at supporting employee well-being and professional growth.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development

Employee assistance programme

Private healthcare

Mental health programmes

Cycle to work scheme

Season Ticket Loan

Flexible working

Qualifications

• Experience in pharmaceutical or agency writing required.
• Strong analytical and interpretation skills.
• Experience with regulatory submissions worldwide.

Responsibilities

• Analyze, interpret, and critique complex scientific data for regulatory submissions.
• Manage projects and client relations effectively.

Skills

Project Management

Client Management

Education

Life-science Graduate

PhD or Research Experience

Job description

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Regulatory Medical Writer, Wolverhampton

Client: Complete Regulatory | An IPG Health Company

Location: Wolverhampton

Job Category: Other

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EU work permit required: Yes

Job Views:

7

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 combining science, creativity, and technology to deliver exceptional medical communications solutions.

What do we do?

We provide high-quality clinical documentation support to the pharmaceutical industry, including clinical study reports, protocols, summaries, overviews, regulatory responses, and more across various therapy areas.

The role

We seek Regulatory Writers with clever and curious minds. Relevant experience in pharmaceutical or agency writing is essential. Applicants should be life-science graduates, ideally with a PhD or research experience, though not mandatory.

You will analyze, interpret, and critique complex scientific data for regulatory submissions worldwide. Strong project management and client management skills are also required.

What will you get in return?

This role offers valuable experience in regulatory writing within a supportive, reputable team. You will be part of a larger organization with world-class services and flexible structures.

Benefits include:

• Flexible Time Off – uncapped paid time off
• Retail and gym discounts
• Training and development
• Employee assistance programme
• Private healthcare
• Headspace and MYNDUP mental health programmes
• 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 reasonable adjustments are needed during the application process.