Senior Clinical Research Associate

ICON Clinical Research, LP

Sydney, Australia
Fully remote
Monitor clinical trial sites
Conduct site visits
Collaborate with cross-functional teams
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards

Job Summary

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance.
  • ICON is committed to providing a workplace free of discrimination and harassment, offering equal consideration for employment.

Matching Summary

Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

Skills & Requirements

Must-have

  • Monitor clinical trial sites
  • Conduct site visits
  • Collaborate with cross-functional teams
  • Provide training and guidance
  • Build and maintain relationships

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Shape the future of clinical development

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate in Australia
  • Proven ability to manage multiple sites
  • Proficiency in clinical trial software
  • Ability to travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter