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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
Nova Medical Services
The Clinical Research Coordinator manages the planning and execution of clinical trials, ensuring strict adherence to ICH, GCP, and regulatory guidelines. Key duties include coordinating patient visits, maintaining regulatory documentation, and managing study data entry and verification.
$23 - $25 / HOUR
18 days ago
ALX Oncology Inc.
Supports clinical operations by managing the Trial Master File (TMF), coordinating site activation, and tracking study documents. Collaborates with CROs and internal teams to ensure regulatory compliance and efficient trial execution.
$100,000 - $120,000 / YEAR
29 days ago
