Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Manage a portfolio of clinical studies and identify study risks when new studies start .

Posted 10/22/2026full-timeRemote • IndiaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical studies, performing risk assessments, and utilizing analytics to derive actionable insights from data. Proficient in developing mitigation plans and maintaining effective communication with stakeholders in the pharmaceutical and healthcare sectors.

Highest-signal resume keywords

Clinical Study ManagementRisk AssessmentData AnalysisAdvanced Excel ProficiencyClient-Facing Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ExtractionData VisualizationMonitoring Package DevelopmentCorrective Action PlanningLaboratory Metrics Reporting

Soft Skills

Effective CommunicationInfluencing SkillsPriority ManagementProblem-SolvingCollaboration

Certifications & Qualifications

Master’s DegreePhD

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryRisk Management PlansContinuous Process ImprovementStakeholder Engagement

About the role

Key responsibilities & impact

Manage a portfolio of clinical studies and identify study risks when new studies start
Develop mitigation plans for identified study risks
Identify issues in study data and suggest internal or external corrective and preventive actions
Create 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
Monitor and report clinical study laboratory metrics
Extract data from multiple sources, analyze it, and present actionable 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 identify study issues and proactively address risks
Liaise with Developers to ensure monitoring tools meet client specifications
Maintain regular communication with key stakeholders
Support creation and maintenance of Risk Management Plans
Participate in continuous process improvements, functional meetings, and process updates
Support quality, productivity, and compliance with internal strategy

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
Strong working proficiency in English
Ability to extract information from multiple data sources and convert raw data into actionable insights
Ability to perform risk assessments and propose monitoring solutions
Ability to use analytics and visualizations to review study laboratory data
Ability to communicate effectively and influence others
Ability to manage conflicting priorities and dynamic timelines
Ability to operate with minimal guidance and own deliverables end-to-end

Benefits

Comp & perks

Equal Opportunity Employer commitment
Consideration of qualified applicants without regard to protected characteristics
Assistance with online job application tools and accommodations for individuals with disabilities