Medical Writer / Senior Medical Writer (Remote)

Meet Life Sciences; Ramsbottom; Remote; GBP 50,000 - 70,000; Full time

Job summary

A leading medical communications agency in the UK is seeking an experienced Senior Medical Writer / Medical Writer for a remote position. The role involves developing high-quality scientific publications and requires a strong understanding of regulatory compliance. Ideal candidates thrive in fast-paced environments and are skilled in interpreting complex clinical data. Competitive compensation is offered for this key role.

Qualifications

• Proven experience as a Medical Writer within a publications-focused team.
• Strong understanding of regulatory compliance guidelines.
• Ability to manage multiple projects and deadlines.

Responsibilities

• Develop, write, and edit high-quality scientific publications.
• Ensure content meets industry standards and client expectations.
• Interpret and communicate complex clinical data clearly.

Skills

Scientific writing

Medical communications

Collaboration

Data interpretation

Job description

Job Description

Job Title: Senior Medical Writer / Medical Writer (Publications) – Remote, UK

About the Role

We are seeking an experienced Senior Medical Writer / Medical Writer to join our publications-focused team within a leading medical communications agency . This fully remote position (UK-based) offers the opportunity to work across high-value scientific publications, strategic communication plans, and global medical affairs initiatives for top-tier pharmaceutical clients.

You will play a key role in delivering high-quality, scientifically robust content while collaborating closely with internal teams, clients, key opinion leaders (KOLs), and external authors. This role suits someone who thrives in a fast-paced agency environment, values scientific accuracy, and enjoys taking ownership of publication deliverables.

Key Responsibilities

Scientific Content Development

• Develop, write, and edit high-quality scientific publications including manuscripts, abstracts, posters, slide decks, and congress materials.
• Ensure all content meets industry standards, client expectations, and relevant compliance guidelines (e.g., GPP, ICMJE).

Interpret and communicate complex clinical data with clarity, accuracy, and appropriate scientific rigor.