Medical Writer II, Oncology

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.

Responsibilities

• 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

Requirements

• 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