Remote Central Monitor: RBM & Data Risk Analytics

IQVIA

United States

Remote

USD 80,000 - 120,000

Full time

14 days+
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Job summary

IQVIA is seeking a highly analytical Central Monitor to support risk-based monitoring across global clinical studies. This home-based role emphasizes centralized review of risk signals, trend analysis, and clear recommendations to ensure data quality and patient safety.

The position collaborates with CRAs, study teams, and sponsor Risk Advisors to drive risk mitigation and continual process improvement, with strong English communication and data visualization skills.

Qualifications

  • Bachelor’s degree in Life Sciences.
  • Experience with Centralized Monitoring Review, RBM and Clinical Data Analytics.
  • Advanced written and verbal English mandatory; strong presentation skills.
  • Proficiency with Microsoft Excel, reporting tools and data visualization platforms.

Responsibilities

  • Perform centralized monitoring for multiple global studies (4–5 simultaneously).
  • Review site-level and study-level risk signals from centralized monitoring platforms.
  • Analyze clinical/operational data to identify trends, anomalies and risks.
  • Complete signal reviews within 5 business days of signal generation.
  • Document findings and risk assessments clearly with recommended actions.
  • Provide actionable risk mitigation recommendations to study teams and CRAs.
  • Track identified risks and ensure actions are addressed.
  • Prepare study reports, metrics, dashboards and presentations for risk monitoring.
  • Collaborate with sponsor Risk Advisors and cross-functional teams.
  • Support continuous improvement of centralized monitoring processes.

Skills

Centralized Monitoring
Clinical Data Review
RBM
Clinical Data Analytics
Central Monitoring Findings Review
Advanced English
Presentation Skills
Excel
Reporting Tools
Data Visualization

Education

Life Sciences degree

Tools

Excel

Job description

IQVIA is seeking a highly analytical Central Monitor to support risk-based monitoring across global clinical studies. This home-based role emphasizes centralized review of risk signals, trend analysis, and clear recommendations to ensure data quality and patient safety.

The position collaborates with CRAs, study teams, and sponsor Risk Advisors to drive risk mitigation and continual process improvement, with strong English communication and data visualization skills.

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