Independent Drug Monitoring, Manager

IQVIA UK

Base: $93,100.00 - $232,800.00 annualized; bonus/e...
Not specified
6 years clinical trial operations experience
Knowledge of ich-gcp and regulatory guidelines
Experience managing unblinded drug oversight processes
The Independent Drug Monitoring Manager position at IQVIA UK involves overseeing unblinded drug management for clinical trials globally, ensuring compliance with protocols and regulatory guidelines. The ideal candidate should have extensive experience in clinical trial operations, strong leadership skills, and a proactive approach to risk management

Job Summary

  • The role is responsible for unblinded drug management on a global scale, ensuring key trial milestones are met.
  • Candidates must lead study teams in managing drug oversight processes while maintaining the blind and ensuring inspection readiness.
  • The position requires developing documentation, training materials, and overseeing Independent Drug Monitors to address investigational product activities.

Matching Summary

Match Score: 85

The Independent Drug Monitoring Manager position at IQVIA UK involves overseeing unblinded drug management for clinical trials globally, ensuring compliance with protocols and regulatory guidelines. The ideal candidate should have extensive experience in clinical trial operations, strong leadership skills, and a proactive approach to risk management.

Salary

Base: $93,100.00 - $232,800.00 annualized; Bonus/Equity: Incentive plans may be offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • 6 years clinical trial operations experience
  • Knowledge of ICH-GCP and regulatory guidelines
  • Experience managing unblinded drug oversight processes
  • Ability to maintain study blind integrity
  • Strong communication with global stakeholders

Nice-to-have

  • Project management experience preferred
  • Pharmacy or monitoring background preferred
  • Global level work experience preferred
  • Proactive solution-oriented approach
  • Experience with IVRS and EDC system setup

Key Requirements

  • Bachelor's degree in scientific or business discipline
  • 6 years relevant experience in clinical trial operations
  • Willingness to travel locally/domestically as needed

Work Rights

Not specified

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