💼 About This Role

You'll lead centralized monitoring and risk-based quality management for clinical trials. You'll ensure data integrity and proactively manage study risks. This role offers independent oversight of complex studies.

🎯 What You'll Do

• Conduct risk assessments and develop mitigation strategies for clinical studies.
• Perform centralized statistical monitoring to detect data anomalies.
• Support monthly RBQM meetings and coordinate data cleaning activities.
• Prepare reports and presentations on monitoring findings and recommendations.

📋 Requirements

• Bachelor's degree in life sciences, statistics, data management, or clinical operations.
• Minimum 2 years experience in clinical monitoring or trial management.
• Working knowledge of ICH GCP guidelines and clinical development process.
• Proficiency in statistical analysis and data monitoring tools.