Clinical Research Associate II Job at ICON, Tampa, FL

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  • ICON
  • Tampa, FL

Job Description

Clinical Research Associate II position supporting oncology trials in a sponsor-dedicated model. The role involves site monitoring, regulatory compliance, and data management across the southeast region with up to 75% travel requirement.

Responsibilities

  • Serve as primary liaison between investigational sites and sponsor
  • Conduct site visits including selection, initiation, monitoring, and close-out activities
  • Monitor patient safety and ensure timely adverse event and serious adverse event reporting
  • Maintain documentation in CTMS and eTMF; resolve data queries and track compliance records
  • Support subject recruitment and retention; oversee investigational drug accountability

Requirements

  • Bachelor's degree in Life Sciences or RN qualification
  • 2+ years on-site monitoring experience in pharmaceutical or CRO industry
  • Experience monitoring oncology trials, including prostate and lung cancer
  • Proficiency in ICH-GCP, CTMS, and eTMF systems
  • Eligible to work in United States without visa sponsorship
  • Ability to travel 60-75% across southeast region; Tampa-based preferred

Job Tags

Visa sponsorship

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