Central Monitor II

📋 Description

• Central monitoring of clinical trial data quality and integrity
• Lead RBQM plan development and risk assessments
• Collaborate with functions to identify KRIs and monitor data
• Conduct centralized statistics monitoring and remote data review
• Prepare reports and sponsor communications
• Mentor junior colleagues and help develop processes

🎯 Requirements

• Bachelor’s in life sciences/stats/data/clinical ops or equivalent
• At least 2 years in clinical monitoring or trial management
• Working knowledge of ICH GCP and clinical development
• Excellent communication, organizational and English skills
• Ability to work independently or in a team and learn data extraction
• Proficiency in statistical analysis and data monitoring tools

🎁 Benefits

• Competitive benefits package
• Opportunities for process improvement and career growth
• Collaborative, cross-functional team environment