Full-time

Data Verification Specialist - Laval Site

Posted by Charles River Laboratories • June 13, 2026

📍 laval (administrative region), qc, Canada
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Description

Contribute to quality data management at Charles River’s Laval site as a Data Reviewer focused on clinical pathology. Utilize your analytical skills to promote best practices in data collection.
In this permanent, full-time role, you will verify the completeness and integrity of complex clinical pathology data. The position demands expertise in Good Laboratory Practices (GLP) and adherence to regulatory agency requirements. Candidates should possess a college diploma in science along with three years of relevant experience, showcasing flexibility and the ability to thrive under deadlines.
Key Responsibilities:
• Conduct thorough reviews of clinical pathology supporting data
• Ensure compliance with GLP and IACUC rules
• Maintain data integrity throughout studies
• Educate others on data collection best practices
• Work independently while meeting project deadlines
Requirements:
• Requires a college diploma in science
• At least 3 years of GLP experience

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