Clinical Research Associate Job at ICON, Texas

  • ICON
  • Texas

Job Description

Clinical Research Associate II role at a global contract research organization focused on sponsor-dedicated clinical trial monitoring. Responsibilities include site management, protocol compliance oversight, data quality assurance, and cross-functional collaboration throughout the trial lifecycle.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and close-out activities for clinical trials
  • Ensure protocol adherence, data integrity, and patient safety throughout trial execution
  • Collaborate with investigators and site personnel to support effective study operations
  • Review trial data and resolve outstanding queries to maintain data 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 understanding of clinical trial processes, regulations, and ICH-GCP guidelines
  • Strong organizational and communication abilities with meticulous attention to detail
  • Capacity to work independently and collaboratively in fast-paced settings
  • Willingness to travel approximately 60% as required
  • Legal right to work in the country where role is based

Job Tags

Contract work

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