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University of Miami
Overview
The coordinator manages simple clinical research protocols, including participant screening, data collection, and maintenance of regulatory binders. They are responsible for recruiting patients, obtaining informed consent, and ensuring adherence to international and local regulatory standards.
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Compensation
Salary not listed
Posted
26 days ago
Cedars-Sinai
Assist in the coordination and implementation of noncomplex research studies through data collection and participant scheduling. Support regulatory compliance by assisting with IRB submissions and maintaining GCP and HIPAA standards.
$24 - $33 / HOUR
1 month ago
Vanderbilt University
The Research Specialist is responsible for conducting in vivo experiments, managing rodent colonies, and performing DMPK assays. They also handle general laboratory operations, including supply ordering and the training of new personnel.
The Clinical Research Associate I coordinates clinical study implementation, abstracts research data, and ensures compliance with federal and institutional regulations. They are responsible for completing case report forms, managing regulatory submissions to the IRB, and assisting with patient research billing.
