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Central Monitor II

  • Mid level
  • Full time
  • 2+ years

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About the role

Precision Medicine Group provides clinical solutions for clinical research and development. The Central Monitor II assesses study risk, reviews trial data, and supports risk-based quality management and issue resolution.

What you'll do

  • Conduct clinical study risk assessments and develop mitigation strategies
  • Analyze study data to identify anomalies, trends, and risks
  • Support monthly RBQM meetings and coordinate data-cleaning activities
  • Monitor operational metrics and communicate issues to study teams
  • Prepare reports and recommendations for sponsors and study teams

Skills

Must have

Nice to have

  • Central monitoring
  • CRO experience

Who it's for

Education
Bachelor's degree
Degree
life sciences, statistics, data management, clinical operations
Experience
2+ years
Languages
english
Domain
clinical trials

About Precision Medicine Group

Precision Medicine Group has 15 open roles in Bangalore, at Precision for Medicine India HQ. See every Precision Medicine Group role.

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