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IQVIA
Overview
The Clinical Research Associate will monitor and manage clinical trial sites to ensure strict adherence to study protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, overseeing recruitment plans, managing documentation, and providing training to site staff.
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Compensation
$71,900 - $189,000 / YEAR
Posted
2 days ago
ICON plc
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data entry and site documentation.
Salary not listed
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
$71,900 - $169,300 / YEAR
10 days ago
Lurie Children's Hospital
Coordinates clinical research activities including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing while overseeing study supplies and financial invoicing.
$49,920 - $81,619 / YEAR
15 days ago
Serve as the primary contact between investigation sites and sponsors while conducting various site visits to ensure compliance with ICH-GCP and SOPs. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.
18 days ago
Serve as the primary contact between investigational sites and sponsors while conducting various site visits to ensure compliance with regulations. Responsibilities include monitoring patient safety, overseeing drug accountability, and managing data quality and site documentation.
$91,336 - $114,170 / YEAR
