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Clinical Research Associate

ICON · CA +1 more

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Clinical OperationsFull-time$91k–$114kCompany career page

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Role summary

Clinical Research Associate position focused on hematology/oncology monitoring activities in California or Colorado. This sponsor-dedicated role involves conducting site visits, ensuring protocol compliance, and maintaining data integrity for clinical trials within ICON's global organization.

What they're looking for

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 2 years experience as Clinical Research Associate
  • 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
  • Located in California or Colorado near major airport; willing to travel 60-75% regionally

What you'll be doing

  • Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensure protocol compliance, data integrity, and patient safety throughout trial process
  • Collaborate with investigators and site staff to facilitate 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

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