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AstraZenecaNew
Overview
The CRA is responsible for monitoring study conduct at allocated sites to ensure proper delivery and compliance with international guidelines and local regulations. Key tasks include site initiation, monitoring visits, data verification, and managing study supplies and documentation.
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Compensation
CA$109,149 - CA$143,258 / YEAR
Posted
New
WELL Health Diagnostic Centres
Coordinate day-to-day clinical trial activities, including participant recruitment, data management, and regulatory submissions to the Research Ethics Board. Manage study visits, perform clinical assessments like vitals and sample collection, and liaise with sponsors and internal departments.
CA$100,000 - CA$120,000 / YEAR
1 month ago
Everest Clinical Research
The Clinical Trial Assistant will interact with sponsors, sites, and vendors to ensure timely and high-quality operationalization of clinical trials while compiling and reviewing documentation for site qualification and regulatory submissions. Responsibilities also include setting up, maintaining, and archiving essential documents in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
CA$45,000 - CA$65,000 / YEAR
2 months ago
