Clinical Data Risk & Solutions Analyst – Global Monitor

• Manage a portfolio of clinical studies as Global Monitor
• Identify study risks and develop mitigation plans with internal teams
• Identify issues in study data and recommend corrective and preventive actions
• Develop customized, study-specific monitoring packages
• Assess which laboratory samples are at risk of not being resulted on time
• Select appropriate monitoring offerings and write clear monitoring instructions
• Monitor and report clinical study laboratory metrics
• Extract information from multiple data sources and convert raw data into actionable insights
• Present key findings to internal and external stakeholders
• Perform risk assessments on low-complexity studies with the Global Study Manager and Study Design Lead
• Use analytics and visualizations to review study laboratory data and proactively address risks
• Liaise with Developers to ensure monitoring tools meet client specifications
• Maintain stakeholder communication and support Risk Management Plan creation and maintenance
• Participate in process improvements, functional meetings, and keeping processes current
• Comply with internal strategy and support quality and productivity

• Master’s Degree or PhD in a scientific field
• 10 years of related experience in project management or data analysis for the pharmaceutical/healthcare industry; education can substitute for work experience
• Advanced knowledge of Excel
• Previous client-facing experience
• Strong working proficiency in English
• Ability to operate with minimal guidance while owning deliverables end-to-end
• Ability to communicate ideas/concepts effectively and motivate/influence others
• Robust self-organization and ability to manage conflicting priorities
• Ability to create and motivate a team around project deliverables

• Equal Opportunity Employer
• Accessibility accommodations for applicants with disabilities
• Data privacy information provided through Labcorp’s Privacy Statement