Senior Clinical Research Associate

ICON

Multiple Locations
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity assurance
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.
  • As a Senior Clinical Research Associate, you will ensure clinical trials are conducted according to protocol, regulatory requirements, and industry standards while safeguarding participant safety and data integrity.
  • ICON offers competitive salaries and a range of benefits focused on well-being and work-life balance, 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 assurance
  • Site management and performance assessment
  • Clinical trial software proficiency
  • Stakeholder relationship management

Nice-to-have

  • Cross-functional team collaboration
  • Training and guidance provision
  • Problem-solving skills
  • Inclusive and diverse work culture
  • Work-life balance focus

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Valid driver’s license
  • Strong understanding of regulatory requirements
  • Proven multi-site and project management

Work Rights

Not specified

Tailored Resume

Cover Letter