Medical Writer II, Oncology

Johnson & Johnson · High Wycombe, UK

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Medical AffairsFull-timeCompany career page

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Role summary

Medical Writer II supporting oncology regulatory documentation at Johnson & Johnson. The role involves authoring clinical and regulatory documents across early- to late-stage compounds, working within cross-functional teams in a hybrid setting across multiple international locations.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-06 (originally posted 2026-10-06). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Medical writing experience in pharmaceutical industry or clinical research
Knowledge of regulatory guidelines and clinical document standards
Proficiency with medical writing style guides, templates, and SOPs
Strong written and verbal communication skills
Ability to work collaboratively in matrix team environments
Experience with clinical study reports, protocols, or investigator brochures

What you'll be doing

Write and coordinate clinical documents including protocols, study reports, and investigator brochure updates
Perform quality control, literature searches, and prepare document components under supervision
Lead or participate in cross-functional document planning and review meetings
Manage document timelines, scheduling, and project tracking activities
Mentor junior staff on processes, document planning, and content as experience level allows

Key requirements

Therapeutic area: Oncology

Privacy & handoff

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What RoleLantern checked

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Date posted1 day ago

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Salary listedNeeds clarity

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