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Clinical Research Associate 2, IQVIA

IQVIA · Durham, NC

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Clinical OperationsFull-time$75k–$198kCompany career page

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Role summary

IQVIA seeks a Clinical Research Associate II to conduct on-site monitoring for clinical trials across multiple therapeutic areas. The role involves site management, regulatory compliance, monitoring activities, and cross-functional collaboration to support study success.

What they're looking for

  • Bachelor's degree
  • Minimum 1 year independent on-site monitoring experience in CRO, biotech, or pharmaceutical
  • Working knowledge of GCP, ICH, and clinical trial regulations
  • Strong communication, organizational, and problem-solving skills
  • Proficiency with Microsoft Office applications

What you'll be doing

  • Conduct site selection, initiation, routine monitoring, and closeout visits per regulatory requirements
  • Build relationships with investigative sites and provide protocol and study-specific training
  • Monitor study progress including site activation, patient recruitment, enrollment, and data quality
  • Maintain study documentation, regulatory records, and Trial Master File compliance
  • Prepare monitoring reports and support patient recruitment and retention efforts

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