Senior Cra

ICON

Copenhagen, Denmark
Fully remote
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and site management
Senior CRA at ICON Plc plays a critical role in overseeing clinical trial activities ensuring data integrity, participant safety, and compliance throughout the study lifecycle

Job Summary

  • Senior CRA at ICON Plc plays a critical role in overseeing clinical trial activities ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
  • ICON offers a competitive salary along with a range of benefits focused on well-being and work-life balance including health insurance, retirement planning, and global employee assistance programs.
  • ICON is committed to an inclusive and accessible environment, providing equal employment opportunities without discrimination and reasonable accommodations for disabilities.

Matching Summary

Senior CRA at ICON Plc plays a critical role in overseeing clinical trial activities ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and site management
  • Cross-functional team collaboration
  • Travel at least 60% internationally and domestically
  • Valid driver's license

Nice-to-have

  • Strong organizational and problem-solving skills
  • Excellent communication and interpersonal skills
  • Stakeholder management and influence
  • Training and guidance provision
  • Inclusive and diverse work culture

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Ability to manage multiple sites and projects
  • Proficiency in clinical trial software and tools
  • Ability to travel at least 60%
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter