(Senior) Clinical Research Associate (CRA)

IQVIA · Taipei City, Taiwan

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate for site monitoring and management in clinical trials. Responsible for conducting monitoring visits, managing recruitment, ensuring protocol adherence, and maintaining regulatory compliance across assigned study sites.

What they're looking for

Bachelor's degree in scientific or healthcare discipline
Minimum 1 year of on-site clinical trial monitoring experience
Knowledge of GCP and ICH guidelines
Proficiency with Microsoft Office (Word, Excel, PowerPoint)
Strong written and verbal English communication skills
Organizational and problem-solving abilities

What you'll be doing

Conduct site selection, initiation, monitoring, and close-out visits per protocol requirements
Collaborate with sites on subject recruitment planning and enrollment tracking
Evaluate study site compliance with protocol and regulatory standards
Maintain Trial Master File and Investigator's Site File documentation per GCP standards
Generate monitoring reports, follow-up letters, and track data quality issues

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Date posted16 days ago

Last source check1 day ago

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