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IQVIA
Overview
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.
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Compensation
CA$84,000 - CA$170,900 / YEAR
Posted
17 days ago
Care Access
The Clinical Research Coordinator, RN conducts delegated clinical tasks and monitoring of research participants while ensuring strict adherence to Good Clinical Practices (GCP) and protocol compliance. Key duties involve patient coordination, obtaining informed consent, performing clinical procedures like blood draws and ECGs, and managing investigational products.
Salary not listed
20 days ago
The Senior Site Activation Coordinator will execute country-level tasks related to site activation, including performing feasibility studies and managing document review, tracking, and distribution for investigative sites. This role ensures all activities comply with applicable regulations, SOPs, and project guidelines while supporting system and database maintenance.
CA$51,200 - CA$85,300 / YEAR
1 month ago
