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JENAVALVE TECHNOLOGY INC
Overview
Supports Clinical Research Associates in managing site start-up, maintenance, and close-out activities for clinical projects. Ensures the accuracy and compliance of study-related documents according to GDP and regulatory standards.
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Compensation
$29 / HOUR
Posted
6 days ago
ICON plc
You will conduct clinical trial monitoring activities, including site visits and data review to ensure protocol compliance and patient safety. Additionally, you will collaborate with investigators and site staff while contributing to the preparation of essential study documentation.
Salary not listed
23 days ago
The Clinical Research Associate serves as the primary point of contact for investigational sites, ensuring compliance with ICH-GCP and regulatory standards. They are responsible for conducting site visits, monitoring patient safety, managing data integrity, and overseeing drug accountability.
The Clinical Research Associate serves as the primary point of contact for investigational sites, conducting site visits to ensure compliance with ICH-GCP and regulatory standards. They are responsible for monitoring patient safety, managing site documentation, and overseeing drug accountability throughout the clinical trial process.
$91,336 - $114,170 / YEAR
1 month ago
IQVIA
The Clinical Research Associate performs site monitoring visits to ensure study protocols, regulations, and sponsor requirements are strictly followed. They manage site progress, including recruitment, data integrity, and regulatory documentation to ensure high-quality study execution.
$71,900 - $189,000 / YEAR
The Senior CRA is responsible for monitoring and managing clinical sites to ensure strict adherence to study protocols, regulatory requirements, and sponsor expectations. They will conduct various site visits, facilitate subject recruitment, and maintain essential study documentation to ensure high-quality clinical research data.
$87,200 - $169,300 / YEAR
