Sr. Clinical Research Associate

ICON

Multiple Locations
Clinical trial site monitoring
Good clinical practice (gcp) standards
Site performance assessment
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to fostering an inclusive environment driving innovation and excellence.
  • As a Senior Clinical Research Associate, you will play a critical role in overseeing clinical trial activities to ensure data integrity, participant safety, and compliance throughout the study lifecycle.
  • 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 fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • site performance assessment
  • clinical trial software proficiency
  • travel up to 60% internationally and domestically
  • valid driver’s license

Nice-to-have

  • cross-functional team collaboration
  • training and guidance provision
  • stakeholder management skills
  • influence and drive compliance
  • inclusive and accessible environment

Key Requirements

  • advanced degree in life sciences, nursing, or medicine
  • extensive CRA experience
  • ability to manage multiple sites and projects
  • valid driver’s license
  • travel at least 60% of the time

Work Rights

Not specified

Tailored Resume

Cover Letter