CRA Job at ICON, Portland, OR

  • ICON
  • Portland, OR

Job Description

Clinical Research Associate II position in Portland, OR supporting sponsor-dedicated clinical trial monitoring. Responsibilities include site qualification, protocol compliance oversight, data integrity management, and regulatory documentation preparation within a collaborative, fast-paced environment.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out activities
  • Ensure protocol compliance, data integrity, and patient safety throughout trials
  • Collaborate with investigators and site staff on study conduct
  • Review data and resolve queries to maintain clinical data quality
  • Prepare and review study documentation including protocols and reports

Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 2 years clinical research associate experience
  • Comprehensive knowledge of clinical trial processes, ICH-GCP regulations
  • Strong organizational, communication, and attention to detail skills
  • Ability to work independently and collaboratively
  • Willingness to travel approximately 60% as required
  • Legal right to work in United States

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