Clinical Research Associate Job at ICON, Kentucky

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  • ICON
  • Kentucky

Job Description

ICON seeks a Clinical Research Associate II for the East Coast region to support sponsor-dedicated clinical trial operations. The role involves monitoring activities, ensuring protocol compliance, and maintaining data integrity across multiple study sites in a fast-paced environment.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits
  • Ensure protocol compliance, data integrity, and patient safety throughout trials
  • Collaborate with investigators and site staff to facilitate study conduct
  • Perform data review and resolve queries to maintain clinical data quality
  • Contribute to preparation and review of study documentation and reports

Requirements

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

Job Tags

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