Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Manage a portfolio of clinical studies as Global Monitor .

Posted 10/22/2026full-timeRemote • IndiaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical studies, including risk assessment, data analysis, and stakeholder communication. Proficient in utilizing analytics and visualizations to derive actionable insights from laboratory data while ensuring compliance with quality standards.

Highest-signal resume keywords

Clinical Study ManagementData AnalysisRisk AssessmentAdvanced Excel SkillsClient-Facing Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ExtractionMonitoring Package ImplementationLaboratory Metrics ReportingAnalytics and VisualizationCorrective and Preventive Actions

Soft Skills

Problem-Solving SkillsCustomer Service SkillsSelf-OrganizationCommunication SkillsTeam Motivation

Certifications & Qualifications

Master’s DegreePhD

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryProject ManagementRisk ManagementContinuous Process Improvement

About the role

Key responsibilities & impact

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 suggest corrective and preventive actions
Implement 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
Communicate regularly with key stakeholders
Support Risk Management Plan creation and maintenance
Contribute to continuous process improvements and functional meetings
Keep processes up to date and comply with internal strategy
Support quality and productivity improvements

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
High quality standards and attention to detail
Strong motivation, flexibility and creativity
Problem-solving and customer service skills
Ability to operate with minimal guidance and own 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
Strong working proficiency in English

Benefits

Comp & perks

Equal Opportunity Employer
Accommodation assistance for individuals with disabilities
Consideration of qualified applicants regardless of protected characteristics