Regulatory Medical Writer

JR United Kingdom; Stoke-on-Trent; On-site; GBP 30,000 - 50,000; Full time

Job summary

A leading company is seeking a Regulatory Medical Writer in Stoke-on-Trent. This role demands solid experience in pharmaceutical writing along with excellent communication and organizational skills. You will support the pharmaceutical industry by analyzing complex scientific data and managing various projects, while enjoying flexible working and substantial career growth opportunities.

Benefits

Flexible Time Off – uncapped paid time off

Retail and gym discounts

Excellent training and development

Employee assistance programme

Private healthcare

Headspace and MYNDUP mental health programmes

Cycle to work scheme

Season Ticket Loan

Flexible working

Qualifications

• Relevant writing experience in the pharmaceutical industry is essential.
• Excellent communication and organizational skills needed.
• Project management skills for handling multiple projects required.

Responsibilities

• Analyze and interpret complex scientific data for regulatory submissions.
• Manage multiple projects efficiently.
• Provide writing support and consultancy to the pharmaceutical industry.

Skills

Communication

Project Management

Organizational Skills

Education

Life-science degree (PhD preferred)

Job description

Regulatory Medical Writer, Stoke-on-Trent

Client:

Complete Regulatory | An IPG Health Company

Location:

Stoke-on-Trent, United Kingdom

Job Category:

Other

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 celebrated and awarded Med Comms agencies. We are 800 experts combining science, creativity, and technology to create exceptional medical communications solutions for our clients.

What do we do?

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

The role

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

You will need excellent communication and organizational skills to analyze, interpret, and critique complex scientific data used in regulatory submissions worldwide. Project management skills are essential for managing multiple projects efficiently, and client management skills are needed to resolve issues promptly.

What will you get in return?

This role is ideal for those looking to build experience in regulatory writing within a supportive, reputable team. You will be part of a larger organization offering world-class services and flexible organizational structures.

Long-term career development opportunities include:

• Flexible Time Off – uncapped paid time off
• Retail and gym discounts
• Excellent training and development
• Employee assistance programme
• Private healthcare
• Headspace and MYNDUP mental health programmes
• Cycle to work scheme
• Season Ticket Loan
• Flexible working

How to Apply or Contact Us

Apply by clicking the link below.

IPG Health Medical Communications values diversity and encourages applicants from all backgrounds and abilities. Please let us know if any reasonable adjustments are needed to support your application process.