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ICON plc
Overview
The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. It also requires ensuring protocol compliance, data integrity, and collaborating with investigators to maintain high-quality clinical data.
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Compensation
Salary not listed
Posted
2 days ago
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.
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 Senior CRA is responsible for conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They also collaborate with site staff and contribute to the preparation of study documentation and clinical study reports.
The role involves conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and patient safety. Additionally, the CRA will collaborate with site staff and perform data review to maintain high-quality clinical trial documentation.
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.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will collaborate with site staff and investigators while performing data review to maintain high-quality clinical documentation.
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.
25 days ago
Kelonia Therapeutics
The Medical Director will support clinical development activities for oncology programs, including medical monitoring, safety review, and data analysis. They will also contribute to key clinical deliverables such as study protocols, investigator brochures, and regulatory submission documents.
$243,000 - $291,000 / YEAR
1 month ago
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.
Medpace, Inc.
The Medical Writer will write IND and NDA modules, clinical study reports, protocols, and amendments. They will also coordinate quality control reviews and interact closely with sponsors and subject matter experts.
