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ICON plc
Overview
The Senior Clinical Research Associate will conduct site qualification, monitoring, and close-out visits while ensuring protocol compliance and data integrity. They will also collaborate with investigators and contribute to the preparation of study documentation and clinical reports.
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Compensation
Salary not listed
Posted
17 days ago
The Senior Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with site staff and investigators to facilitate study conduct and prepare essential study documentation.
The US Oncology Network
Responsible for managing research regulatory and administrative activities for clinical trials, including site qualification and document management. Collaborates with investigators and central operations to ensure compliance with SOPs, GCP, and federal regulations.
25 days ago
The Clinical Research Associate is responsible for conducting site qualification, monitoring, and close-out visits to ensure protocol compliance and patient safety. They also collaborate with site staff to facilitate study conduct and perform data review to maintain high-quality clinical data.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and data integrity. Additionally, you will collaborate with site staff and investigators to facilitate study conduct and maintain high-quality clinical data.
1 month ago
Krystal Biotech
The role involves managing clinical trial supplies, monitoring investigative sites for GCP compliance, and maintaining the Trial Master File. Additionally, the associate will train site staff and collaborate with finance to track study budgets and invoices.
