Perform ongoing, in-depth review of clinical trial data across multiple studies (e.g., EDC, IVRS, safety, central laboratory databases)
Identify data inconsistencies, missing data, protocol deviations, and outliers at patient and site level
Manage simultaneous data review across multiple small trials, ensuring consistency in oversight
Review and initiate targeted queries for critical or inconsistent data points
Provide clear, actionable feedback to avoid repetitive errors
Detect protocol deviations through data review
Act as a central point of contact for data-related issues
Work closely with: Data Management, Biostatistics, Medical Monitoring, and Pharmacovigilance

Be rewarded with market-related salary and benefits package
Skills development
We offer various internal and external employee and leadership trainings, trainee programs and digital solutions

Clinical Trial Manager – Central Monitoring

Key skills