Clinical Research Associate

ICON · Long Beach, CA +1 more

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

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Role summary

ICON Strategic Solutions seeks a Clinical Research Associate to support oncology trials in the Western region. The role involves site monitoring, protocol compliance oversight, and data quality management across sponsor-dedicated clinical programs.

What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 2 years of clinical research associate monitoring experience
Oncology monitoring experience required
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to travel 60-75% within assigned region

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 processes
Collaborate with investigators and site staff to facilitate study conduct
Review data and resolve queries to maintain clinical data quality
Prepare and review study documentation including protocols and clinical study reports

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