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ICON plc
Overview
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
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Compensation
Salary not listed
Posted
8 days ago
The Senior Clinical Research Associate monitors clinical study progress at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. They are responsible for ensuring that clinical trials are accurately conducted, recorded, and reported according to SOPs and ICH-GCP standards.
CA$108,576 - CA$135,720 / YEAR
17 days ago
