Senior Medical Writer & Regulatory Strategy Lead

GSK; Fir Tree; On-site; GBP 90,000 - 120,000; Full time

Job summary

GSK is seeking a Principal Medical Writer who will lead and deliver high‑quality medical writing for complex clinical and regulatory projects. You will work closely with clinical, regulatory, statistical, and cross‑functional teams.

We value scientific rigor, clear communication, collaboration, and ownership. This role offers visible impact, professional growth, and meaningful work that aligns with GSK's mission to unite science, technology and talent to get ahead of disease together.

Qualifications

• Bachelor's degree in life sciences or related field.
• 5+ years in medical or regulatory writing within pharma/healthcare.
• 3+ years of CTD dossier development experience.
• 3+ years authoring clinical protocols and regulatory submission documents.

Responsibilities

• Lead authoring and strategic planning for clinical and regulatory documents.
• Manage end-to-end writing projects with contributors and timelines.
• Translate complex clinical data into clear scientific narratives for diverse audiences.
• Act as SME on medical writing standards and regulatory expectations.
• Support KPI tracking, process improvement, and audit readiness.

Skills

Medical writing

Regulatory writing

Clinical study reports

CTD dossiers

ICH guidelines

GCP

Education

Bachelor's degree in life sciences

Advanced degree in life sciences

Job description

GSK is seeking a Principal Medical Writer who will lead and deliver high‑quality medical writing for complex clinical and regulatory projects. You will work closely with clinical, regulatory, statistical, and cross‑functional teams.

We value scientific rigor, clear communication, collaboration, and ownership. This role offers visible impact, professional growth, and meaningful work that aligns with GSK's mission to unite science, technology and talent to get ahead of disease together.