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Ergomed
Overview
Perform pre-study, initiation, interim, and close-out monitoring visits to ensure site adequacy and compliance. Mentor junior staff and verify that investigators have the necessary qualifications and resources to conduct clinical studies.
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Compensation
Salary not listed
Posted
3 days ago
ICON plc
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.
$110,520 - $138,150 / YEAR
4 days ago
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.
9 days ago
