Join Charles River Laboratories as a Data Reviewer in Clinical Pathology in Laval. Your primary responsibility will be to ensure data completeness and compliance with Good Laboratory Practices (GLP).

This role requires extensive review of clinical pathology data while adhering to both regulatory and best practice standards. With a minimum of three years in a GLP setting, you will bring your expertise as a flexible and independent worker capable of meeting deadlines. Your efforts will enhance the quality and integrity of our clinical studies.

Key Responsibilities:
• Verify complex clinical pathology data for accuracy
• Ensure compliance with GLP, SOPs, and regulatory rules
• Maintain integrity and quality across studies
• Advocate for best practices in data collection processes
• Handle responsibilities under time constraints

Requirements:
• Minimum 3 years’ experience in GLP
• Ability to adapt to changing ...