Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Manage a portfolio of clinical studies as a 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 developing monitoring strategies and ensuring compliance with project management standards in the pharmaceutical and healthcare sectors.

Highest-signal resume keywords

Clinical Study ManagementData AnalysisRisk AssessmentProject ManagementClient-Facing Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data-Driven Analytical ThinkingAdvanced ExcelMonitoring Package ImplementationLaboratory Data ReviewCorrective and Preventive Actions

Soft Skills

Problem-Solving SkillsAttention to DetailEffective CommunicationSelf-OrganizationTeam Motivation

Tools & Technologies

Monitoring ToolsAnalytics SoftwareData Visualization Tools

Industry Keywords

Pharmaceutical IndustryHealthcare IndustryGlobal Project ManagementContinuous ImprovementQuality Standards

About the role

Key responsibilities & impact

Manage a portfolio of clinical studies as a Global Monitor
Identify study risks and develop mitigation plans with internal teams when new studies start
Identify issues in study data and suggest internal or external corrective and preventive actions
Implement customized, study-specific monitoring packages based on study needs and client requests
Assess laboratory sample risks and select appropriate monitoring offerings
Write clear monitoring instructions for handoff to another team
Comply with the CCLS Global Project Management strategy
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 laboratory data and proactively address risks
Liaise with Developers to ensure monitoring tools meet client specifications
Maintain regular communication with key stakeholders
Support Risk Management Plan creation and maintenance
Participate in process improvements, functional meetings, and process updates
Support continuous improvement, quality, and productivity initiatives

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 problem-solving and customer service skills
Ability to operate with dynamic timelines and changing priorities
Ability to work with minimal guidance and own deliverables end-to-end
Ability to effectively communicate ideas/concepts 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
Consideration for qualified applicants regardless of protected characteristics
Accommodation assistance for individuals with disabilities during the application process