Job Description & How to Apply Below
A leading clinical research organization in Canada is seeking a TMF Coordinator to manage Trial Master File processes throughout the study lifecycle. The ideal candidate will have a college diploma and 1-3 years of relevant experience, emphasizing TMF organization and regulatory compliance. Responsibilities include ensuring the TMF is complete and ready for inspection, providing training, and maintaining quality assurance standards.
This full-time role offers the flexibility to work from home with occasional office visits.
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Position Requirements
10+ Years
work experience
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