Senior Cra

ICON

Paris, France
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and compliance
Senior CRA at ICON Plc plays a critical role in overseeing clinical trial activities to ensure 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 to ensure data integrity, participant safety, and compliance throughout the study lifecycle.
  • ICON offers a diverse culture that rewards high performance and nurtures talent with competitive salary and benefits focused on well-being and work-life balance.
  • ICON is committed to providing an inclusive and accessible environment free of discrimination and harassment, encouraging all qualified applicants to apply.

Matching Summary

Senior CRA at ICON Plc plays a critical role in overseeing clinical trial activities to ensure 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 compliance
  • Site management and performance assessment
  • Travel up to 60% internationally and domestically
  • Valid driver’s license

Nice-to-have

  • Cross-functional team collaboration
  • Training and guidance provision
  • Stakeholder relationship building
  • Problem-solving skills
  • Strong communication and interpersonal skills

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

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