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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
Coordinate the setup and monitoring of oncology clinical trials while maintaining accurate study documentation and reports. Build collaborative relationships with investigators and site staff to ensure patient safety and regulatory compliance.
15 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
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 recorded and reported in accordance with ICH-GCP and standard operating procedures.
Monitor the progress of clinical studies at investigative sites or remotely to ensure compliance with protocols and regulatory requirements. Maintain accurate records and reports in accordance with ICH-GCP and standard operating procedures.
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.
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
21 days ago
IQVIA
Coordinate clinical research studies by performing complex clinical procedures and managing subject well-being. Responsibilities include recruiting volunteers, administering study drugs, and ensuring data accuracy in accordance with protocols.
CA$40 - CA$50 / HOUR
25 days ago
