💼 About This Role

You'll lead clinical trial site activation and regulatory submissions for a precision medicine CRO. Your work directly impacts site activation readiness and ensures compliance with ICH-GCP and local regulations. You'll mentor junior staff and drive process improvements across global studies.

🎯 What You'll Do

• Drive country-level submissions and site activation processes.
• Prepare Clinical Trial Application forms and submission dossiers.
• Maintain project plans, trackers, and regulatory intelligence tools.
• Manage essential documents for site activation and IMP release.

📋 Requirements

• Bachelor's degree in life sciences or related field.
• 5+ years of regulatory or start-up specialist experience in CRO/pharma.
• Fluency in English and Turkish.
• Experience with computerized information systems and electronic spreadsheets.