Join our TMF Operations team as a TMF Coordinator focused on ensuring quality and compliance in Trial Master File documentation. This role supports clinical trials through effective document management and collaboration.

We're seeking a detail-oriented TMF Coordinator to manage TMF documentation adhering to global regulations. Your responsibilities will include maintaining a comprehensive TMF structure, ensuring inspection readiness, and enhancing collaboration with cross-functional teams. This position offers the prospect to contribute to essential clinical trial management.

Key Responsibilities:
• Maintain TMF structures and ensure compliance with regulations
• Support inspection readiness and audit activities effectively




• Accurately file and manage TMF documents within our systems
• Perform quality control checks on TMF documents
• Collaborate with study teams to ensure documentation is complete

Requirements:
• Bachelor’s degree in Life Sciences or related field
• 1-3 years of TMF management experience
• Knowledge of eTMF platforms and regulations
• Strong attention to detail and organizational skills
• Ability to work remotely and manage multiple tasks

Bring your expertise in TMF management and compliance to drive clinical trial success.
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📌 TMF Coordinator for Clinical Trials (Quebec City)
🏢 Alimentiv
📍 Quebec City