Clinical Trial Coordinator: Docs, Budgets & Site Ops
Listed on 2026-10-12
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Science
Clinical Research
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.
As a Clinical Trial Coordinator:
Docs, Budgets & Site Ops, you will play an important part at ICON Strategic Solutions in Canada.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Clinical Trial Coordinator:
Docs, Budgets & Site Ops role at ICON Strategic Solutions, based in Canada.
We are looking to fill the Clinical Trial Coordinator:
Docs, Budgets & Site Ops position at ICON Strategic Solutions in Canada.
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