Sr Cra / Csm

ICON

Milan, Italy
Clinical trial site monitoring
Regulatory compliance management
Good clinical practice (gcp) standards
Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards

Job Summary

  • Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
  • ICON offers a diverse culture that rewards high performance and nurtures talent with a range of benefits focused on well-being and work-life balance.
  • ICON is committed to providing an inclusive and accessible environment for all candidates and a workplace free of discrimination and harassment.

Matching Summary

Senior CRA at ICON Plc plays a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

Skills & Requirements

Must-have

  • clinical trial site monitoring
  • regulatory compliance management
  • Good Clinical Practice (GCP) standards
  • data integrity assurance
  • site performance assessment
  • international and domestic travel
  • valid driver’s license

Nice-to-have

  • cross-functional team collaboration
  • training and guidance provision
  • stakeholder relationship management
  • problem-solving skills
  • organizational skills
  • communication and interpersonal skills
  • inclusive work environment

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter