Clinical Research Associate Job at ICON, Georgia

  • ICON
  • Georgia

Job Description

ICON seeks a Clinical Research Associate II to conduct clinical trial monitoring activities in Georgia, including site qualification, protocol compliance oversight, and data integrity management. The role involves travel and collaboration with investigators to support efficient study operations.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout trial process
  • Collaborate with investigators and site staff to facilitate smooth study conduct
  • Perform data review and resolution of queries to maintain high-quality clinical data
  • Prepare and review study documentation including protocols and clinical study reports

Requirements

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

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