Clinical Site Manager Ii

ICON

Mechelen, Belgium
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and compliance
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The Senior CRA role involves monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and GCP standards while supporting successful trial execution.
  • ICON offers competitive salary and a range of benefits focused on well-being, work-life balance, and inclusion, including health insurance, retirement planning, and global employee assistance programs.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and compliance
  • Multiple site and project management
  • International and domestic travel
  • Valid driver’s license

Nice-to-have

  • Cross-functional team collaboration
  • Training and guidance provision
  • Stakeholder relationship management
  • Strong organizational and problem-solving skills
  • Excellent communication and interpersonal skills
  • Inclusive and diverse work culture

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Ability to travel at least 60% internationally and domestically
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

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