FSP - Central Monitor in Mexico
Core
Centralized review of study and site-level risk signals to identify trends, assess issues, and recommend actions for data quality and patient safety in global clinical studies.
Role type
Central Monitor (Clinical Research)
Builds
Risk mitigation strategies and study oversight reports
Domain
Clinical Research / Life Sciences
Deliverable
dashboards & analysis
Required skills
Centralized monitoring review, Risk-based monitoring (RBM), Clinical data analytics, Signal assessment, Trend analysis, Data visualization, Microsoft Excel
Responsibilities
Review site-level and study-level risk signals, Analyze clinical and operational data for anomalies, Document findings and risk assessments, Provide recommendations for risk mitigation, Track follow-up on identified risks, Prepare study reports and metrics dashboards
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