Central Monitor

ICON Clinical Research, LP

Bulgaria
Fully remote
Centralized monitoring execution
Risk identification and management
Data review and reporting
ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • You will play a key role in overseeing and supporting clinical trials through centralized monitoring activities, ensuring data quality, identifying potential risks, and enhancing trial oversight.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • centralized monitoring execution
  • risk identification and management
  • data review and reporting
  • collaboration with study teams
  • adherence to risk-based monitoring plans
  • clinical trial development understanding

Nice-to-have

  • fostering inclusive environments
  • leveraging AI and analytics
  • understanding diverse cultural contexts
  • therapeutic area knowledge

Key Requirements

  • ≥ 5 years pharmaceutical industry experience
  • ≥ 3 years central monitoring experience
  • Strong clinical trial development understanding
  • Thorough understanding of GCP/ICH standards
  • Data and Digital expertise

Work Rights

Not specified

Tailored Resume

Cover Letter