CRA I

ICON · Zhengzhou, China

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate I position based in ICON's Taipei office with flexibility. The role involves managing clinical trial site operations, ensuring protocol compliance and data integrity, and collaborating with investigators to support study conduct.

What they're looking for

Bachelor's degree in scientific or healthcare-related field
Minimum 2 years experience as a Clinical Research Associate
Knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to travel 60% domestically and internationally with valid driver's license

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

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Date posted2 days ago

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