Regulatory Medical Writer

JR United Kingdom; Cheltenham; On-site; GBP 35,000 - 50,000; Full time

Job summary

A renowned company in medical communications is looking for Regulatory Writers who possess sharp analytical skills and relevant experience. This position involves the analysis of complex scientific data for regulatory submissions and provides growth in regulatory writing within a supportive team. Benefits include uncapped paid time off, private healthcare, and flexible working arrangements.

Benefits

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 agency writing is essential.
• Candidates should preferably have a PhD or research background.
• Ability to analyze, interpret, and critique complex scientific data.

Responsibilities

• Analyze, interpret, and critique complex scientific data for regulatory submissions.
• Handle multiple projects and resolve issues promptly.
• Provide writing support and consultancy to the pharmaceutical industry.

Skills

Communication

Organizational Skills

Project Management

Education

Life-science degree

PhD or research background

Job description

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Complete Regulatory | An IPG Health Company

Location:

Job Category:

Other

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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, known for 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 top-tier writing support and consultancy 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, curious minds. Relevant experience in pharmaceutical or agency writing is essential. Candidates should be life-science graduates, preferably with a PhD or research background, though this is not mandatory.

You will analyze, interpret, and critique complex scientific data for regulatory submissions worldwide, requiring excellent communication and organizational skills. Project and client management skills are also important for handling multiple projects and resolving issues promptly.

What will you get in return?

This role offers growth in regulatory writing within a supportive, reputable team and access to a larger organization with diverse services and flexible structures. Benefits include:

• 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

Click the link below to apply.

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