Become a TMF Operations Coordinator, responsible for the quality and compliance of Trial Master Files. Your detail-oriented skills will ensure our documentation meets rigorous standards.

In this role, you will maintain the completeness and compliance of TMF documentation crucial for clinical trials. Collaborating with study teams, you will manage essential documentation while ensuring readiness for inspections. Your organizational and communication skills will be vital in supporting audit activities and improving TMF workflows across projects and teams.

Key Responsibilities:
• Maintain in-depth TMF knowledge and compliance
• Classify and index TMF documents accurately
• Perform quality control checks on TMF content
• Investigate and resolve documentation discrepancies
• Support effective stakeholder communication

Requirements:
• Robust organizational and time-management abilities
• Familiarity with eTMF systems and tools
• Detail orientation focused on quality control
• Effective collaboration skills across functions
• Ability to manage multiple projects simultaneously

Advance your career in clinical research management with a focus on quality TMF practices.
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📌 TMF Operations Coordinator Role (Ontario)
🏢 Alimentiv
📍 Ontario