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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
Montefiore Health System
Oversee multiple clinical trials and quality improvement projects within the Neurology department, serving as the primary contact for patients and study teams. Ensure strict adherence to study protocols and regulatory requirements from the FDA, NIH, and Institutional Review Boards.
$53,040 - $66,300 / YEAR
10 days ago
Glaukos
The CRA is responsible for assessing, training, and monitoring clinical research sites to ensure data integrity and protocol compliance. This includes conducting site visits, managing investigator relationships, and overseeing the accountability of investigational products.
$73,600 - $85,000 / YEAR
11 days ago
Systimmune
The CRA II manages and oversees clinical study sites to ensure data quality and patient safety in compliance with ICH-GCP and local regulations. Key duties include performing site visits, managing patient recruitment, and maintaining the Trial Master File.
$80,000 - $110,000 / YEAR
23 days ago
Tekton Research Inc
The Clinical Research Coordinator II manages daily operations of assigned clinical trials, ensuring compliance with protocols and regulatory policies. Key duties include coordinating with sponsors, managing study documentation, and performing clinical procedures for study participants.
29 days ago
