Clinical Trial Coordinator: Docs, Budgets
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ICON plc in Canada seeks a detail-oriented Clinical Operations Associate to support budgeting, document management, site administration, and cross-country coordination. You will help prepare budgets, contracts, and study submissions while ensuring compliant processes across CTMS/eTMF systems.
You will manage on-site sponsor presence two days a week in Kirkland, collaborate with investigators and vendors, and maintain high standards of GCP compliance and data integrity.
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