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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
National Research Council Canada
Control of materials including raw materials, finished products, and critical consumables. Support quality control activities focusing on testing and release of materials. Review of documentation, SOPs, and data. Coordinate with external laboratories and internal teams. Environmental monitoring data entry. Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results. Improve QC activities through SOP modifications
CA$83,435 - CA$107,838 / YEAR
2 days ago
Canadian Blood Services
Perform routine laboratory testing, accessioning, and reporting of results while managing blood component inventory. Maintain laboratory equipment and ensure all activities comply with operating procedures and regulatory requirements.
CA$37 - CA$37 / HOUR
7 days ago
Perform routine and specialized immunohematology testing, including blood grouping and antibody identification for patient and donor samples. Manage laboratory inventory, prepare reagents, and ensure equipment maintenance according to regulatory requirements.
8 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
GSK
The student will support the Quality Control department by managing the archiving and circulation of GMP documents. They will also act as an administrator for the eSOP system and assist users with document layout and technical issues.
Salary not listed
1 month ago
The student will support the Quality Control department by managing document archiving, circulation, and identification within the documentation center. They will also act as an administrator for the eSOP system and assist users with document formatting and compliance.
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
Groupe JAMP Pharma
The Documentation Technician ensures the maintenance and proper functioning of the documentation management system and the archiving/retention program, adhering to applicable regulatory requirements and internal procedures. Daily tasks involve managing documentation system tasks such as processing requests, numbering, maintaining registers, formatting, issuing, withdrawing, distributing, and archiving quality system documents.
