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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
18 days ago
Chartwell
Responsible for the well-being of residents and the administration of required medical care. Collaborates with nurses, doctors, and other healthcare professionals to monitor and report changes in resident health status.
Salary not listed
22 days ago
Organon
The MSL is responsible for engaging in non-promotional, peer-to-peer scientific communications with Scientific Leaders and Key Decision Makers. They provide medical information, gather disease insights, and support internal medical affairs plans and clinical trial identification.
CA$103,600 - CA$153,600 / YEAR
1 month 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
The role involves performing monitoring and site management tasks for various clinical protocols, therapeutic areas, and sites, including conducting site visits (selection, initiation, monitoring, and close-out) according to contractual scope and regulatory guidelines. Key duties include managing protocol training, tracking study progress, ensuring data quality and integrity, and maintaining essential study documentation like the TMF and ISF.
CA$102,500 - CA$170,900 / YEAR
3 months ago
