Senior Cra

ICON Clinical Research, LP

MidWest, United States
Monitoring clinical trial sites
Adherence to study protocols
Good clinical practice (gcp) standards
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence.
  • Responsibilities include monitoring clinical trial sites, conducting site visits, collaborating with cross-functional teams, providing training, and building relationships with site personnel.
  • ICON offers competitive salary, various annual leave entitlements, health insurance, retirement planning, a global employee assistance program, and life assurance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization focused on fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • Monitoring clinical trial sites
  • Adherence to study protocols
  • Good Clinical Practice (GCP) standards
  • Oncology monitoring experience
  • Travel at least 60% of the time

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Shaping the future of clinical development
  • Well-being and work life balance

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites
  • Proficiency in relevant clinical trial software
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

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