Senior Global Clinical Study Manager Job at IQVIA, Indianapolis, IN

  • IQVIA
  • Indianapolis, IN

Job Description

Senior Global Clinical Study Manager responsible for end-to-end planning and execution of clinical trials across multiple regions. Oversees site management, enrollment, monitoring, and closeout while managing stakeholder relationships, budgets, and regulatory compliance.

Responsibilities

  • Lead site selection, activation, recruitment performance, and monitoring strategy throughout study lifecycle
  • Serve as primary client contact and manage cross-functional teams across regions and cultures
  • Develop integrated study plans, identify risks, and implement mitigation and corrective actions
  • Manage study budgets, forecasting, billing reviews, and financial performance tracking
  • Ensure compliance with GCP standards, protocols, regulatory requirements, and trial management file health

Requirements

  • Bachelor's degree in life sciences or related field
  • 5+ years clinical research/monitoring experience with 2+ years in study management
  • 2+ years global study management across multiple countries and regions
  • Phase I–III clinical trial experience with Phase III required
  • Oncology experience required
  • Strong ICH-GCP and FDA regulatory knowledge
  • Demonstrated project financial management and Microsoft Office proficiency

Compensation: $93,100–$232,800 base

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