Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Manage an assigned portfolio of clinical studies .

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 managing clinical studies, performing risk assessments, and utilizing analytics to derive actionable insights from data. Proficient in stakeholder communication and fostering a culture of continuous improvement within the pharmaceutical and healthcare sectors.

Highest-signal resume keywords

Clinical Study ManagementRisk AssessmentData AnalysisClient-Facing ExperienceAdvanced Excel Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ExtractionData VisualizationMonitoring SolutionsLaboratory Metrics ReportingProject Management

Soft Skills

Problem-SolvingCustomer ServiceEffective CommunicationTeam MotivationConflict Management

Tools & Technologies

Monitoring ToolsAnalytics Software

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryRisk Management PlansContinuous ImprovementStakeholder Engagement

About the role

Key responsibilities & impact

Manage an assigned portfolio of clinical studies
Work with internal teams to identify study risks and develop mitigation plans
Identify issues in study data and suggest internal or external corrective and preventive actions
Put customized, study-specific monitoring packages in place based on study needs or 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
Monitor and report clinical study laboratory metrics
Extract and analyze information from multiple data sources and present key findings to internal and external stakeholders
Perform risk assessments on low-complexity studies before study start 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 and functional meetings
Keep processes up to date and comply with internal strategy
Support a culture of continuous improvement, quality, and productivity

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/visualizations to review study laboratory data
Ability to work with developers on monitoring tools
Strong problem-solving and customer service skills
Ability to operate with minimal guidance and own deliverables end-to-end
Ability to communicate ideas effectively and motivate/influence others
Ability to manage conflicting priorities and dynamic timelines
Ability to create and motivate a team around project deliverables

Benefits

Comp & perks

Meaningful work contributing to improving health and improving lives
Career growth opportunities
Equal employment opportunity and inclusive workplace
Accessibility accommodations for applicants with disabilities