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ICON plcNew
Overview
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Oversee patient safety, drug accountability, and data quality while collaborating with cross-functional clinical teams.
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Compensation
CA$110,520 - CA$138,150 / YEAR
Posted
New
AstraZenecaNew
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.
CA$109,149 - CA$143,258 / YEAR
Translational Research in Oncology
Responsible for processing and quality reviewing study documentation for the electronic Trial Master File (eTMF) according to SOPs and GCP guidelines. Provides administrative support to the TMF Manager through reporting, metrics, and document metadata assignment.
CA$37,000 - CA$41,000 / YEAR
15 days ago
AstraZeneca
The Clinical Research Associate (CRA) is responsible for the local delivery of clinical studies at assigned sites, acting as the main contact for monitoring study conduct to ensure proper delivery according to guidelines and regulations. This involves preparing, initiating, monitoring, and closing assigned sites, training site staff, driving site performance, and ensuring data quality and compliance.
23 days ago
The Clinical Research Associate is locally responsible for study delivery at assigned sites, acting as the main contact to monitor study conduct, ensuring compliance with AZ procedures and international guidelines like ICH-GCP. Key tasks include preparing, initiating, monitoring, and closing sites, training site staff, driving site performance, and ensuring timely data quality and reporting.
3 months ago
