🛠 Tech Stack

💼 About This Role

You'll support clinical study sites and project teams by managing essential documents, tracking data in CTMS, and liaising with investigators. You'll ensure compliance with ICH-GCP and regulatory requirements while enabling efficient trial execution and remote site oversight.

🎯 What You'll Do

• Collect and review essential documents for Trial Master File.
• Maintain site data in CTMS and track study milestones.
• Act as site contact for study management and issue escalation.
• Assist with investigator recruitment and feasibility activities.

📋 Requirements

• Bachelor's degree in business, scientific, or healthcare discipline.
• Minimum 1 year of relevant clinical research experience.
• Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint).
• Fluency in French and English (verbal and written).