Back to jobsPerforming medical writing tasks for regulatory documents including HA consultation packages, bridging reports, and clinical summaries
Proofreading Chinese version documents to ensure accuracy and regulatory compliance
Taking overall responsibility to drive local clinical trial disclosure on specific trials and projects
Collaborating with cross-functional teams to gather and synthesise complex scientific information
Contributing to knowledge sharing and skill building initiatives across the medical writing community
Building strong relationships with stakeholders and colleagues to ensure alignment and quality
Managing timelines and deliverables to support critical regulatory submissions
