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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
Indero
The Senior CRA monitors clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP guidelines. Responsibilities include conducting site visits, performing source data verification, and potentially mentoring other CRAs as a Lead CRA.
Fortrea
The role involves managing all aspects of clinical site monitoring, including initiation, routine visits, and close-out for oncology trials. Key duties include ensuring patient safety, verifying informed consent, and maintaining data integrity through CRF review and SAE reporting.
9 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 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.
17 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
Responsible for all aspects of study site monitoring, including routine visits, close-outs, and site management. Ensures the protection of study patients and the integrity of data submitted on Case Report Forms.
1 month 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
IQVIA
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
