Clinical Data Integrity Specialist
5 days ago
The Central Monitor II plays a pivotal role in ensuring the integrity and quality of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.
- Key Responsibilities:
- Study Risk Assessment: Conduct thorough risk assessments for clinical studies, identifying potential issues and developing mitigation strategies in consultation with functional team leads and PMs.
- Centralized Statistical Monitoring: Perform centralized statistical monitoring & data analysis on study data to detect anomalies, trends, and potential risks, ensuring data accuracy and compliance.
- RBQM Meetings: Support monthly RBQM meetings by reviewing study data, documenting findings, action plans, and coordinating data cleaning activities to support study deliverables.
- Data Quality Assurance: Ensure the highest standards of data quality and integrity through proactive monitoring and timely interventions.
- Collaboration: Work closely with clinical operations, data management, biostatistics, and other departments to support proactive oversight and management and data cleaning for studies.
- Reporting: Prepare detailed reports and presentations on monitoring activities, findings, and recommendations for sponsors and study teams.
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Clinical Data Specialist
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Key Healthcare Data Integration Specialist
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Clinical Document Specialist
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Data Integration Specialist
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Clinical Data Specialist
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Lead Clinical Specialist in Digital Health
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