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ICON plc
Overview
The Sr. CRA is responsible for managing investigative sites and performing monitoring activities throughout the clinical trial lifecycle to ensure data integrity and subject safety. Key duties include conducting site visits, managing essential documents, and ensuring compliance with protocols and regulatory standards.
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Compensation
$110,520 - $138,150 / YEAR
Posted
2 days ago
Ardelyx
The Clinical Research Associate II provides sponsor oversight of assigned investigative sites, focusing on high-quality protocol execution and compliance with GCP and regulatory requirements. This role involves monitoring site performance through data review, supporting all phases of the clinical trial lifecycle, and ensuring timely collection and maintenance of essential regulatory documents.
$99,000 - $121,000 / YEAR
2 months ago
Laborie Medical Technologies Corp
The Senior Clinical Research Associate oversees site management activities, including site selection, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also serve as a primary liaison between internal teams, vendors, and clinical sites to drive patient enrollment and maintain high-quality data standards.
Salary not listed
4 months ago
