Clinical Research Associate Job at ICON, Florida

  • ICON
  • Florida

Job Description

ICON is hiring a Clinical Research Associate II in Miami, Florida to monitor cardio and obesity clinical trials in a sponsor-dedicated model. The role involves site management, protocol compliance, data integrity oversight, and cross-functional collaboration with investigators and site staff to support innovative treatment development.

Responsibilities

  • Conduct site qualification, initiation, monitoring, and closeout 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 resolve 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 meticulous attention to detail
  • Ability to work independently and collaboratively in fast-paced environment
  • Willingness to travel approximately 60% as required

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