Senior Central Monitor

📋 Description

• Review the protocol and ensure the Integrated Data Review Plan is updated for the central monitor
• Provide recommendations during initial Risk Management meetings on appropriate TA or study specific
• Inspect aggregate clinical and operational data from multiple sources (eCRF, vendor data, digital
• Use Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and Data Anomalies to identify
• Document detected issues and emerging risks.
• Translate the issues and emerging risks by clearly outlining the situation, the significance or

🎯 Requirements

• Bachelor’s degree in related fields including life sciences and risk-based disciplines.
• Minimum of 5 years of clinically related or data trend analysis experience; at least 4 years of
• Experience working in a RBQM model or similar experience with risk-based environment preferred.
• Demonstrated current in-depth knowledge and understanding or willingness to learn of appropriate
• TA experience is preferred in one of the following areas (Neuroscience, Oncology, Immunology, Eye

🎁 Benefits

• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving
• Equal Opportunity Employer/Veterans/Disabled.