Conduct clinical site monitoring across Canada using French fluency, GCP expertise, and source document verification skills. This independent contract is as needed.
The Data Coordination Unit at the Medical University of South Carolina seeks a site monitor located in Canada. The work supports human subject protection, accurate trial data, and compliance with approved protocols, GCP, and regulatory requirements. Candidates should be fluent in spoken and written English and French.
Key Responsibilities: Conduct in office and remote monitoring visits
Verify source documents and generate data queries
Assess investigator and staff compliance
Review investigational product handling and storage
Write reports and close action items
Requirements: Bachelor’s degree in life sciences
At least four years of site monitoring experience
Hospital-based clinical trial experience
Knowledge of clinical development and GCP
Experience with CTMS and medical record systems
Apply your bilingual communication, clinical trial, and monitoring expertise to support compliant studies with DCU across Canada.

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📌 Bilingual Clinical Site Monitor Canada (Manitoba)
🏢 Medical University Of South Carolina
📍 Manitoba