Regulatory Medical Writer

JR United Kingdom; Milton Keynes; On-site; GBP 35,000 - 55,000; Full time

Job summary

A leading company in medical communications seeks a Regulatory Medical Writer in Milton Keynes. The role involves producing clinical documentation for the pharmaceutical sector, requiring strong communication, organizational, and project management skills. Enjoy flexible work arrangements and great employee benefits as part of a supportive team.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Training and development

Employee assistance program

Private healthcare

Mental health programs

Cycle to work scheme

Season Ticket Loan

Flexible working

Qualifications

• Relevant experience in the pharmaceutical industry is essential.
• The role requires excellent communication and organizational skills.
• Project management and client management skills are necessary.

Responsibilities

• Analyze, interpret, and critique complex scientific data for regulatory submissions.
• Handle multiple projects efficiently and resolve client issues promptly.

Skills

Communication

Project Management

Organizational Skills

Education

Life-science degree

PhD or similar research background

Job description

Regulatory Medical Writer, Milton Keynes

Client:

Complete Regulatory | An IPG Health Company

Location:

Milton Keynes

Job Category:

Other

EU work permit required:

Yes

Job Views:

4

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 are 800 experts dedicated to combining science, creativity, and technology to deliver exceptional medical communications solutions.

What do we do?

We provide top-tier writing support and consultancy services to the pharmaceutical industry, producing clinical documentation such as study reports, protocols, summaries, and regulatory responses across various therapy areas.

The role

We seek Regulatory Writers with sharp and curious minds. Relevant experience within the pharmaceutical industry or an agency is essential. Candidates should be life-science graduates, ideally with a PhD or research background, though this is not mandatory.

You will need excellent communication and organizational skills for analyzing, interpreting, and critiquing complex scientific data used in regulatory submissions worldwide. Project management skills are necessary to handle multiple projects efficiently, and client management skills to resolve issues promptly.

What will you get in return?

This role offers a great opportunity to build regulatory writing experience within a supportive, reputable team. You will also be part of a larger organization offering world-class services and flexible work arrangements.

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

How to Apply

Click the link below to apply. We celebrate diversity and encourage applicants from all backgrounds and abilities. Please let us know if any accommodations are needed during the application process.

Join us at IPG Health Medical Communications and be part of creating impactful medical communications that make a difference.