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Medical Writer II, Oncology

Johnson & Johnson · Spring House, PA +1 more

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Medical AffairsFull-time$92k–$148kCompany career page

The apply link worked recently (not employer-confirmed).

Role summary

Medical Writer II supporting oncology regulatory documentation within Johnson & Johnson's Integrated Data Analytics & Reporting business. The role involves authoring diverse regulatory medical writing documents across early- and late-stage compounds, working in cross-functional teams with increasing independence.

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 Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.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 regulatory or clinical documentation
  • Knowledge of pharmaceutical regulatory guidelines and industry standards
  • Proficiency with medical writing tools, systems, and SOPs
  • Strong written and verbal communication skills
  • Ability to work collaboratively in matrix team environments
  • Experience with clinical study reports, protocols, and regulatory submissions

What you'll be doing

  • Author and coordinate clinical documents including protocols, CSRs, and investigator's brochures
  • Conduct quality control, literature searches, and maintain document abbreviations and references
  • Lead cross-functional document planning and review meetings as appropriate
  • Track project timelines, scheduling, and document strategy execution
  • Mentor junior staff and guide team members on medical writing processes and best practices

Key requirements

Therapeutic area
Oncology

Privacy & handoff

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