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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
3 days ago
Ergomed
Conducts pre-study, initiation, interim, and close-out monitoring visits to ensure site adequacy and compliance. Responsible for training site staff and mentoring junior staff through co-monitoring visits.
Salary not listed
8 days ago
