Senior Cra

ICON

Israel
Fully remote
Monitoring clinical trial sites
Good clinical practice (gcp) standards
Clinical trial data integrity
As a Senior CRA at ICON Plc, you will play 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

  • As a Senior CRA at ICON Plc, you will play 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 range of additional benefits focused on well-being and work life balance opportunities for you and your family, including various annual leave entitlements and health insurance offerings.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and the company is committed to providing a workplace free of discrimination and harassment.

Matching Summary

As a Senior CRA at ICON Plc, you will play 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

  • Monitoring clinical trial sites
  • Good Clinical Practice (GCP) standards
  • Clinical trial data integrity
  • Site management and performance assessment
  • Clinical trial software proficiency
  • Travel up to 60% of the time

Nice-to-have

  • Cross-functional team collaboration
  • Training and guidance provision
  • Stakeholder relationship management
  • Inclusive and diverse work culture
  • Bilingual communication in Hebrew and English

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive Clinical Research Associate experience
  • Valid driver’s license
  • Excellent written and verbal communication in Hebrew & English

Work Rights

Not specified

Tailored Resume

Cover Letter