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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
Health Sciences North Research Institute
Oversee and manage clinical research studies across multiple portfolios from start-up to close-out. Coordinate day-to-day operations, data collection, and participant recruitment while ensuring regulatory compliance.
CA$31 - CA$37 / HOUR
11 days ago
Worldwide Clinical Trials
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Salary not listed
14 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.
CA$109,149 - CA$143,258 / YEAR
23 days ago
Centricity Research
Support the execution of clinical research studies by recruiting participants and conducting study visits. Perform laboratory procedures including sample collection, processing, and shipping in compliance with protocols and SOPs.
28 days ago
The Clinical Screening Coordinator leads research-related recruitment initiatives and screens patients for clinical study participation based on protocol criteria. They are responsible for maintaining recruitment logs, managing databases, and performing clinical tasks such as obtaining vital signs and completing source documents.
CA$40,000 - CA$50,000 / YEAR
1 month ago
Everest Clinical Research
The Clinical Trial Assistant will interact with sponsors, sites, and vendors to ensure timely and high-quality operationalization of clinical trials while compiling and reviewing documentation for site qualification and regulatory submissions. Responsibilities also include setting up, maintaining, and archiving essential documents in the Trial Master File (TMF) and Clinical Trial Management System (CTMS).
CA$45,000 - CA$65,000 / YEAR
2 months 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
