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Clinical Research Associate

ICON

ICON Strategic Solutions seeks a Clinical Research Associate II in San Antonio, Texas to support sponsor-dedicated clinical trials in cardiology and obesity. The role involves conducting site monitoring activities, ensuring protocol compliance, and maintaining data integrity across the trial lifecycle.

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 on study conduct
  • Review clinical data and resolve data queries to maintain quality standards
  • Prepare and review study documentation including protocols and clinical study reports

Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 2 years of Clinical Research Associate experience
  • Deep 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 settings
  • Willingness to travel approximately 60% as required
Vacancy posted 1 day ago
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