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Providence Healthcare
Overview
Coordinate clinical trials from start-up to closeout, supporting multiple Principal Investigators within a centralized research model. Manage participant recruitment, screening, and data integrity while ensuring strict adherence to regulatory and ethical standards.
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Compensation
CA$32 - CA$47 / HOUR
Posted
9 days ago
Women's College Hospital
The Research Assistant is responsible for recruiting participants, collecting data through medical records and interviews, and assisting in the analysis of results. They also support the preparation of ethics submissions, manuscripts for scientific journals, and grant applications.
CA$27 - CA$33 / HOUR
15 days ago
IQVIA
The CRA II monitors Phase I-IV clinical trials to ensure compliance with protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, training personnel, and managing site activities from start-up to close-out.
CA$84,000 - CA$170,900 / YEAR
17 days ago
ICON plc
The Clinical Research Associate will monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. They will also collaborate with cross-functional teams to manage data collection, site performance, and stakeholder relationships.
Salary not listed
Centricity Research
The Clinical Research Coordinator will support study execution by performing clinical procedures, managing participant safety, and ensuring compliance with protocols and regulatory requirements. They will also handle recruitment, screening, and data documentation to maintain high standards of study integrity.
1 month ago
LifeLabs
The Medical Lab Technologist is responsible for conducting diagnostic specimen testing, ensuring accurate documentation, and maintaining laboratory safety protocols. They will also participate in workflow problem-solving and contribute to the evaluation and implementation of new laboratory technology.
CA$34 - CA$46 / HOUR
OICR
The Research Ethics Coordinator manages the submission, review, and approval process for research protocols within the Ontario Cancer Research Ethics Board. They serve as the primary liaison between the board and research teams, ensuring compliance with ethical standards and regulations.
CA$70,000 - CA$76,000 / YEAR
