VitalBio 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, robust Excel skills, and familiarity with ICH-GCP. This 12-month onsite contract emphasizes meticulous documentation and effective cross-team