Principal/Head of Medical Writing

Overview

As a Principal Medical Writer, you will lead high-quality scientific documents to support regulatory submissions and publications. You collaborate with clinical, regulatory, and medical affairs teams to translate data into clear narratives. The role is on-site in a collaborative environment that values expertise and innovation. You will shape scientific communication and contribute to improving patient outcomes on a global scale.

Retribuzione / Benefits

competitive salary package (GBP)

flexible options depending on experience

on-site role

collaborative environment

Responsabilità

Lead development and review of clinical and regulatory documents ensuring compliance with industry standards

Manage multiple projects with timelines and deliverables across teams

Build strong working relationships with clinical and regulatory personnel to streamline information flow

Drive innovative approaches to scientific writing for clarity and impact

Analyze and interpret complex data to produce concise documentation

Maintain up-to-date knowledge of regulatory requirements and industry best practices

Requisiti fondamentali

Extensive experience in medical or scientific writing within the life sciences

Proven ability to manage large, complex documentation projects

Excellent understanding of regulatory guidelines and submission processes

Strong communication skills and attention to detail

Proficiency with relevant document management tools and software

Relevant certifications or advanced degrees in life sciences are preferred

Strong communication

Attention to detail

Cross-functional collaboration

Document management tools and software