💼 About This Role

You'll join Precision for Medicine as a Regulatory and Start Up Specialist, supporting clinical trial site activations across Taiwan. Your core impact involves preparing regulatory submissions and coordinating ethics approvals to ensure timely study startup.

🎯 What You'll Do

• Prepare Clinical Trial Application Forms and submission dossiers.
• Manage essential documents for site activation and IMP release.
• Customize site-specific Patient Information Sheets and Informed Consent Forms.
• Track CA/EC submission timelines and update project plans.

📋 Requirements

• Bachelor's degree in life sciences or related field.
• 1+ year as a Regulatory or Start Up Specialist in CRO/pharma.
• Experience with electronic spreadsheets and word processing.
• Fluency in English.