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Clinical Research Associate

$91.34k - $114.17k

ICON

Clinical Research Associate position focused on oncology monitoring within a sponsor-dedicated model across the Western U.S. region. Responsibilities include site qualification, trial monitoring, protocol compliance oversight, and data integrity management for clinical studies.

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 to support study conduct
  • Review data and resolve queries to maintain high-quality clinical data
  • Prepare and review study documentation including protocols and clinical reports

Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 2 years of Clinical Research Associate experience
  • Oncology monitoring experience required
  • In-depth knowledge of clinical trial processes, ICH-GCP guidelines, and regulations
  • Strong organizational and communication skills with attention to detail
  • Ability to travel 60-75% within assigned region
  • Legal authorization to work in the United States

Compensation: $91,336.00-$114,170.00 base

Vacancy posted 16 days ago
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