Senior Cra

ICON

US
Fully remote
Conducting site qualification and monitoring
Ensuring protocol compliance and patient safety
Data review and query resolution
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.
  • As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers competitive salary and a range of benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to shaping the future of clinical development.

Skills & Requirements

Must-have

  • Conducting site qualification and monitoring
  • Ensuring protocol compliance and patient safety
  • Data review and query resolution
  • Collaborating with investigators and site staff
  • Ability to travel at least 60% of the time

Nice-to-have

  • Strong organizational and communication skills
  • Attention to detail
  • Ability to work independently and collaboratively
  • Inclusive and diverse team environment

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 1 year independent monitoring for CRA II
  • Minimum 3 years independent monitoring for Senior CRA
  • In-depth knowledge of clinical trial processes and ICH-GCP guidelines

Work Rights

Not specified

Tailored Resume

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