Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Labcorp

Clinical Data Risk & Solutions Analyst – Global Monitor

Labcorp

. Manage a portfolio of clinical studies as Global Monitor .

Posted 10/15/2026full-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 monitoring packages and utilizing analytics to derive actionable insights from laboratory data.

Highest-signal resume keywords
Clinical Study ManagementData AnalysisRisk AssessmentStakeholder CommunicationProject Management

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

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

Hard Skills
Data AnalysisRisk AssessmentExcelMonitoring Package DevelopmentLaboratory Metrics Monitoring
Soft Skills
Client-Facing ExperienceEffective CommunicationSelf-OrganizationTeam MotivationConflict Management
Tools & Technologies
Monitoring ToolsAnalytics SoftwareData Visualization Tools
Industry Keywords
Pharmaceutical IndustryHealthcare IndustryClinical StudiesProject Management

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 recommend corrective and preventive actions
  • Develop 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
  • Maintain stakeholder communication and support Risk Management Plan creation and maintenance
  • Participate in process improvements, functional meetings, and keeping processes current
  • 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 knowledge of Excel
  • Previous client-facing experience
  • Strong working proficiency in English
  • Ability to operate with minimal guidance while owning 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

Benefits

Comp & perks
  • Equal Opportunity Employer
  • Accessibility accommodations for applicants with disabilities
  • Data privacy information provided through Labcorp’s Privacy Statement