Job Description Summary
Responsible for configuring and managing the Central Monitoring Platform by translating study requirements into data-driven solutions while developing and maintaining Key Risk Indicators (KRIs) Quality Tolerance Limits (QTLs) and Data Quality Analytics/Statistical Monitoring tests to enable proactive risk detection. The role also involves building central monitoring dashboards and reports with accurate data ingestion harmonization and visualization for effective study oversight and acting as a technical cross-functional collaborator by working closely with Central Monitors study teams and stakeholders to ensure data quality and overall trial success.Job Description
Key Responsibilities
Essential Requirement
Skills Desired
Clinical Trials Computer Programming Data Analysis Programming Languages Reporting (Inactive) Statistical AnalysisRequired Experience:
IC
Expert Clinical Programmer • Mumbai, Maharashtra, India
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