Central Monitor II

📋 Description

• Study Risk Assessment: Conduct thorough risk assessments for clinical studies, identifying
• Centralized Statistical Monitoring: Perform centralized statistical monitoring & data analysis
• RBQM Meetings: support monthly RBQM meetings by supporting review of study data, documenting
• Data Quality Assurance: Ensure the highest standards of data quality and integrity through
• Collaboration: Work closely with clinical operations, data management, biostatistics, and other
• Reporting: Prepare detailed reports and presentations on monitoring activities, findings, and

🎯 Requirements

• Bachelor’s Degree in a relevant field (life sciences, statistics, data management, clinical
• Minimum 2 years experience in clinical monitoring, clinical trial management or equivalent
• Working knowledge of ICH GCP guidelines and the clinical development process
• Highly effective oral and written communication skills with the ability to communicate effectively
• Excellent organizational and time management skills
• Excellent written and spoken English, including strong grammar and scientific vocabulary skills