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Clinical Quality Auditor Focused Regulatory Compliance and Training
Job Description & How to Apply Below
Step into a pivotal role as a Clinical Quality Auditor, ensuring regulatory compliance through extensive audit processes. Bring your skills to a hybrid work environment where clinical quality standards are maintained with excellence.
This position requires at least 3 years of experience in the pharmaceutical or clinical research space. You’ll be responsible for executing audits, evaluating responses to findings, and participating in training sessions on GxP-related topics. Your bilingual capabilities will be key in enhancing team communication and operational effectiveness.
Key Responsibilities:
• Implement audits in line with established protocols
• Analyze non-compliance and track CAPA effectiveness
• Engage in sponsor audits and regulatory inspections
• Collaborate on training content development
• Facilitate internal and vendor risk reviews
Requirements:
• Bachelor’s degree in a relevant field required
• Minimum 3 years of experience in clinical quality
• Strong grasp of ICH and FDA guidelines
• Bilingual in French and English for effective communication
• Proficient in Microsoft Office tools
Elevate the standards of clinical compliance and training through your auditing expertise and contribute to impactful research practices.
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