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ICON

Regional United States, United States
Fully remote
Conducting site qualification and monitoring visits
Ensuring protocol compliance and patient safety
Collaborating with investigators and site staff
ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.
  • The role involves conducting site visits, ensuring data integrity, and collaborating with clinical trial teams to advance innovative treatments.
  • ICON offers competitive salaries and a range of benefits focused on well-being, work-life balance, and diversity and inclusion.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to innovation and excellence.

Skills & Requirements

Must-have

  • Conducting site qualification and monitoring visits
  • Ensuring protocol compliance and patient safety
  • Collaborating with investigators and site staff
  • Performing data review and query resolution
  • Ability to travel at least 60% of the time
  • Knowledge of ICH-GCP guidelines

Nice-to-have

  • Strong organizational and communication skills
  • Ability to work independently and collaboratively
  • Attention to detail
  • Experience in study coordinator or nursing roles

Key Requirements

  • Bachelor's degree or equivalent in scientific or health-related field
  • Previous experience as Clinical Research Associate with onsite monitoring
  • In-depth knowledge of clinical trial processes and regulations
  • Valid driver’s license
  • Ability to travel internationally and domestically

Work Rights

Not specified

Tailored Resume

Cover Letter