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ThedaCare
Overview
The Clinical Research Specialist coordinates clinical trials by screening patients for eligibility and managing the informed consent process. They are responsible for accurate data collection, maintaining source documents, and ensuring compliance with federal and institutional regulations.
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Compensation
Salary not listed
Posted
26 days ago
Cedars-Sinai
The coordinator independently manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure strict compliance with FDA and IRB regulations while reporting study progress and accrual data to staff.
$28 - $48 / HOUR
1 month ago
The coordinator manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure compliance with FDA and IRB regulations while reporting study progress and accrual data.
$24 - $40 / HOUR
The Clinical Research Coordinator II independently manages study coordination, including screening patients for eligibility, presenting trial concepts, and handling the informed consent process. Responsibilities also include accurate and timely data collection, documentation, entry, reporting, and ensuring compliance with federal and local agencies like the FDA and IRB.
2 months ago
