Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Monitor and report clinical study laboratory metrics .

Posted 10/23/2026full-timeRemote • IndiaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in data analysis and project management within the pharmaceutical and healthcare sectors, with a strong focus on risk assessment, monitoring solutions, and stakeholder communication. Proficient in developing actionable insights from laboratory metrics and maintaining quality standards in dynamic environments.

Highest-signal resume keywords

Master’s Degree Or PhD In A Scientific Field10 Years Of Related Experience In Project Management Or Data AnalysisAdvanced Level Knowledge Of ExcelData-Driven Analytical ThinkingClient-Facing Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data AnalysisRisk AssessmentLaboratory Metrics MonitoringAnalytics And VisualizationsMonitoring Package DevelopmentProject ManagementProcess ImprovementQuality Standards ComplianceProblem-SolvingCustomer Service

Soft Skills

Attention To DetailFlexibilityCreativityEffective CommunicationSelf-Organization

Tools & Technologies

Monitoring ToolsData Sources

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryRisk Management PlansStakeholder CommunicationContinuous Improvement

About the role

Key responsibilities & impact

Monitor and report clinical study laboratory metrics
Extract information from multiple data sources and convert raw data into meaningful, actionable insights
Present key findings to internal and external stakeholders
Perform risk assessments on low-complexity studies before study start in coordination with the Global Study Manager and Study Design Lead
Propose monitoring solutions to mitigate identified risks
Use analytics and visualizations to review laboratory data, identify issues and proactively address risks
Develop customized, study-specific monitoring packages based on study needs and client requests
Determine which laboratory samples are at risk of not being resulted on time
Select appropriate monitoring offerings and write clear monitoring instructions for handoff to another team
Liaise with developers to ensure monitoring tools meet client specifications
Maintain regular communication with key stakeholders
Support creation and ongoing maintenance of Risk Management Plans
Participate in continuous process improvements and functional meetings
Provide input and keep processes up to date
Comply with internal strategy and support quality, productivity and continuous improvement
Work efficiently in a dynamic environment with changing timelines and priorities

Requirements

What you’ll need

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 level knowledge of Excel
Previous client-facing experience
Data-driven analytical thinking
Strong attention to detail and quality standards
Strong motivation, flexibility and creativity
Problem-solving and customer service skills
Ability to work with ambiguity and switch across studies/portfolios as priorities change
Ability to operate with minimal guidance and own deliverables end-to-end
Ability to communicate ideas/concepts effectively and motivate/influence others
Self-organization and ability to manage conflicting priorities
Ability to create and motivate a team around project deliverables
Strong working proficiency in English

Benefits

Comp & perks

Equal Opportunity Employer
Inclusion and belonging in the workforce
Accommodation assistance for individuals with disabilities
Career growth opportunities
Meaningful work with a real impact on people’s health