Senior Clinical Research Associate

ICON

Sao Paulo, Brazil
Clinical trial site monitoring
Good clinical practice (gcp) standards
Data integrity and site management
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 benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to 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

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Data integrity and site management
  • Travel at least 60% internationally and domestically
  • Valid driver’s license

Nice-to-have

  • Cross-functional team collaboration
  • Training and guidance provision
  • Stakeholder management and communication
  • Problem-solving and organizational skills
  • 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
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter