Regulatory Medical Writer

Complete Regulatory | An IPG Health Company
Ipswich, England
11 months ago
Applications closed

Related Jobs

View all jobs
Spotlight

Director Biostatistics - Hematology

CSL
Spotlight

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL

Principal Medical Writer

GSK Stevenage, United Kingdom
Hybrid

Principal Medical Writer

GSK
Hybrid

Compliance Engineer

JASA TALENT Cheltenham, Gloucestershire, United Kingdom
£45,000 – £50,000 pa On-site

Dir, Clinical Trial and Data Transparency

Pfizer India
Remote

Dir, Clinical Trial and Data Transparency

Pfizer
Remote

Regulatory Affairs Manager

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom
£85,000 – £95,000 pa
Posted
1 Jul 2025 (11 months ago)

Complete Regulatory is part of IPG Health Medical Communications, home to the world’s most awarded and celebrated Med Comms agencies. With over 800 dedicated experts, we combine science, creativity, and technology to craft exceptional medical communications solutions for leading pharmaceutical companies worldwide.


What We Do

We specialize in regulatory writing and consultancy services, providing best-in-class support to the pharmaceutical industry. Our work spans a wide range of high-quality clinical and regulatory documents, including:

  • Clinical Study Reports (CSRs)
  • Protocols and Amendments
  • Clinical Summaries and Overviews (for CTD Modules 2.5 & 2.7)
  • Regulatory responses to health authorities
  • Investigator’s Brochures and other supporting documentation


We work across a variety of therapy areas, partnering with clients at all stages of drug development and submission.


The Role: Regulatory Writer

We’re looking for experienced Regulatory Writers who are both clever and curious, with a passion for science and precision. You’ll play a key role in interpreting and communicating complex scientific data clearly and accurately for regulatory submissions worldwide.


Key Responsibilities

  • Write, edit, and review regulatory documents in accordance with guidelines and client requirements
  • Analyze and interpret scientific data to develop coherent and compliant narratives
  • Collaborate with internal teams and clients to ensure high-quality, timely deliverables
  • Manage multiple projects, timelines, and client expectations effectively
  • Proactively resolve project-related issues and contribute to continuous improvement


What You’ll Bring

  • A degree in a life sciences discipline (PhD or research experience preferred, but not essential)
  • Prior regulatory writing experience in a medical communications company, CRO or Pharma
  • A solid understanding of drug development and regulatory documentation requirements
  • Excellent writing, communication, and organizational skills
  • Ability to work both independently and collaboratively in a fast-paced environment


What You’ll Get in Return

This is an opportunity to advance your career in regulatory writing within a highly specialised, supportive, and reputable team, while benefiting from the broader offerings of IPG Health Medical Communications.


We offer a competitive rewards package, including:

  • Flexible Time Off – uncapped paid leave
  • Private healthcare and life assurance
  • Pension scheme
  • Mental health & wellness support – including Headspace and MYNDUP
  • Training & development opportunities
  • Retail and gym discounts
  • Cycle to work scheme
  • Season ticket loan
  • Employee Assistance Programme
  • Long Service Awards
  • Flexible/hybrid working options


If you’re a detail-oriented writer who thrives on making complex science clear, and you're looking for a fresh challenge in a collaborative and forward-thinking environment, we’d love to hear from you.


To Apply or Contact Us

Apply by clicking the link below.


IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creating exceptional medical communications for our clients. Our people are the beating heart of our organisation, and through the positive culture we champion, our teams create communications that not only have a positive impact for our clients, but also impact on the world around us.


We celebrate diversity and encourage applicants from all whatever their background and/or disability. We want you to have every opportunity to shine and show us your talents, so please reach out and let us know if there are any reasonable adjustments we can make to ensure our assessment process works for you.

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.

Where to Advertise Biotech Jobs in the UK (2026 Guide)

Where to advertise biotech jobs UK in 2026: the specialist boards, academic networks and trade channels that reach biotech R&D and bioprocessing talent. The candidate pool spans life scientists, computational biologists, regulatory specialists and biomanufacturing engineers — each with distinct professional networks and job search behaviours. General job boards reach a broad audience but lack the specificity that biotech professionals expect. Specialist platforms, academic channels and sector-specific communities each serve a different part of the market. This guide, published by BiotechnologyJobs.co.uk, covers where to advertise biotech roles in the UK in 2026, how the main platforms compare, what employers should expect to pay, and what the data says about hiring across different role types.