Medical Writer III, X-TA

Johnson & Johnson seeks a Medical Writer III for regulatory medical writing across multiple therapeutic areas within their Innovative Medicine division. The role involves leading clinical and regulatory document development, cross-functional collaboration, and mentoring junior staff across European locations on a hybrid basis.

Responsibilities

• Write and coordinate clinical and regulatory documents including CSRs, IBs, protocols, RMPs, and regulatory responses
• Lead document planning and review meetings with cross-functional teams including clinical staff
• Establish document timelines and strategies while serving as primary medical writing contact for teams
• Coach and mentor junior staff on document processes, planning, and content; provide peer review
• Participate in and lead process working groups to advance writing standards

Requirements

• University degree in scientific discipline; advanced degree (Masters, PhD, MD) preferred
• At least 6 years pharmaceutical/scientific experience and 4 years medical writing experience
• Excellent written and oral communication skills in English
• Strong project and process leadership capabilities
• Attention to detail and ability to manage complex problems
• Demonstrated learning agility and cross-functional relationship building