Clinical Trials Associate: eTMF & CTMS Coordinator
Vital Bio seeks a detail-oriented clinical operations professional in Oakville, Ontario, to manage eTMF continuity, regulatory documentation, and study trackers. You will ensure audit-ready files and accurate CTMS input while coordinating with site staff and cross-referencing data across systems.
The role requires 0–2 years in clinical research, strong Excel skills, and familiarity with ICH-GCP. This 12-month onsite contract emphasizes meticulous documentation and effective cross-team
As a Clinical Trials Associate: eTMF & CTMS Coordinator, you will play an important part at Vital Bio in Oakville, ON, Canada.
Join Vital Bio and contribute to our ongoing work.
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This posting is for the Clinical Trials Associate: eTMF & CTMS Coordinator role at Vital Bio, based in Oakville, ON, Canada.
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