Medical Writer II, X-TA

Johnson & Johnson seeks a Medical Writer II for regulatory medical writing across multiple therapeutic areas (Oncology, Immunology, Neuroscience, Cardiopulmonary, Specialty Ophthalmology). The role involves authoring clinical and regulatory documents, coordinating cross-functional teams, and supporting early- to late-stage compounds in a hybrid environment across Belgium, Germany, or UK locations.

Responsibilities

• Author and coordinate clinical documents including protocols, case study reports, and investigator's brochures
• Write, contribute to, and coordinate low to medium complexity regulatory documents with supervision
• Perform quality control, literature searches, and maintain document references and abbreviations
• Lead and participate in cross-functional document planning and review meetings
• Mentor junior staff and guide team members on medical writing processes and best practices

Requirements

• University or college degree in a scientific field
• Medical writing experience in clinical and regulatory document preparation
• Knowledge of regulatory guidelines and industry standards
• Proficiency with medical writing tools, systems, and templates
• Strong written and verbal communication skills
• Ability to work in cross-functional team environments