Medical Writer II, Oncology
Johnson & Johnson · Antwerp, Belgium +1 more
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Role summary
Johnson & Johnson seeks a Medical Writer II for regulatory medical writing in oncology. The role involves authoring clinical and regulatory documents within a matrix team environment across multiple European and North American locations on a hybrid basis.
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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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 regulatory or clinical documentation
- Knowledge of clinical study reports, protocols, and regulatory guidelines
- Proficiency with medical writing style guides and standard operating procedures
- Strong written communication and document coordination abilities
- Experience with cross-functional collaboration in drug development
- Familiarity with oncology therapeutic area preferred
What you'll be doing
- Author and coordinate clinical documents including protocols, study reports, and investigator brochures
- Perform quality control, literature searches, and prepare document components with supervision
- Lead or contribute to cross-functional document planning and review meetings
- Manage document timelines, scheduling, and project tracking activities
- Mentor junior staff and provide peer review on document content and processes
Key requirements
- Therapeutic area
- Oncology
Privacy & handoff
This role links to Johnson & Johnson's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.