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Labcorp

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

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

Demonstrates expertise in managing clinical studies, including risk assessment, data analysis, and stakeholder communication. Proficient in developing mitigation plans and utilizing analytics to derive actionable insights from laboratory data.

Highest-signal resume keywords
Clinical Study ManagementData AnalysisRisk AssessmentAdvanced Excel ProficiencyClient-Facing Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Data ExtractionMonitoring Package DevelopmentLaboratory Metrics ReportingAnalytics and VisualizationRisk Management Planning
Soft Skills
Problem-SolvingAttention to DetailEffective CommunicationTeam MotivationCustomer Service
Certifications & Qualifications
Master’s DegreePhD
Industry Keywords
Pharmaceutical IndustryHealthcare IndustryProject ManagementProcess 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
  • Implement customized, study-specific monitoring packages
  • Assess laboratory sample risks and select appropriate monitoring offerings
  • Write clear monitoring instructions for handoff to another team
  • 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 creation and maintenance of Risk Management Plans
  • Participate in process improvements, functional meetings, and keeping processes up to date
  • Comply with internal strategy and support 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
  • Data-driven analytical thinking
  • High quality standards and attention to detail
  • Strong problem-solving and customer service skills
  • Ability to operate with minimal guidance and own deliverables end-to-end
  • Ability to effectively communicate ideas/concepts and motivate/influence others
  • Strong working proficiency in English
  • Ability to manage conflicting priorities
  • Ability to create and motivate a team around project deliverables

Benefits

Comp & perks
  • Equal Opportunity Employer commitment
  • Consideration of qualified applicants without regard to legally protected characteristics
  • Accessibility assistance and reasonable accommodation for applicants with disabilities