Clinical Trials Associate: eTMF & CTMS Coordinator (Oakville)

14 Sep

Vitalbio

Oakville

14 Sep

Vitalbio

Oakville

VitalBio seeks a detail-oriented clinical operations qualified 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

📌 Clinical Trials Associate: eTMF & CTMS Coordinator (Oakville)
🏢 Vitalbio
📍 Oakville

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