Central Monitor II (RBQM / KRI review Exp)

📋 Description

• Support the Central Monitoring Lead with study-specific setup, configuration, and ongoing
• Act as a subject matter resource for RBM data analytical tools and use them to conduct data risk
• Perform centralized monitoring of clinical study data in accordance with the study monitoring plan.
• Maintain oversight of risk parameters and relevant indicators at study, country, and site levels.
• Review Key Risk Indicators (KRIs) and identify trends that may indicate systematic data errors
• Analyse monitoring findings and assess their potential implications for study quality, data

🎯 Requirements

• Minimum 2 years of relevant experience in Central Monitoring or a closely related clinical research
• Practical experience working with Risk-Based Quality Management (RBQM) processes and centralized
• Experience reviewing Key Risk Indicators (KRIs) is strongly preferred.
• Experience with CluePoints or similar clinical data analytics and risk-monitoring platforms is
• Understanding of clinical trial data, monitoring processes, data quality principles, and study
• Ability to analyze complex study data and identify trends, anomalies, systematic errors, and

🎁 Benefits

• Fully remote working opportunity from India.
• Full-time position within a global clinical research and life sciences environment.
• Opportunity to work on international clinical studies and contribute to data quality and
• Exposure to advanced RBQM, centralized monitoring, KRI review, and clinical data analytics
• Opportunities to work with specialist data analytics and risk-monitoring technologies.
• Access to professional development and career progression opportunities.