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ICON plc
Overview
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.
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Compensation
Salary not listed
Posted
2 days ago
American Addiction Centers
Coordinates clinical and administrative aspects of sponsored clinical trials, including subject recruitment, enrollment, and data collection. Acts as the primary liaison between sponsors and investigators while ensuring protocol adherence and regulatory compliance.
$31 - $46 / HOUR
3 days ago
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocols and regulatory guidelines. Key duties include performing clinical procedures, managing study documentation, and mentoring junior coordinators.
$60,000 - $90,000 / YEAR
16 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
$91,336 - $114,170 / YEAR
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 Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
21 days ago
The coordinator is responsible for screening, enrolling, and monitoring clinical research subjects while ensuring strict adherence to protocols and regulatory guidelines. Key duties include performing clinical procedures, managing study documentation, and coordinating with sponsors and investigators.
25 days ago
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.
1 month ago
Laborie Medical Technologies Corp
The Senior Clinical Research Associate oversees site management activities, including site selection, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also serve as a primary liaison between internal teams, vendors, and clinical sites to drive patient enrollment and maintain high-quality data standards.
4 months ago
