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Jefferson Health Plans
Overview
Oversees day-to-day clinical trial activities for Neurology, managing studies from startup through closeout. Responsibilities include patient screening, consenting, data management, and ensuring compliance with GCP and federal regulations.
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Compensation
Salary not listed
Posted
11 days ago
Duke Careers
The specialist will support clinical research operations by managing participant documentation, data collection, and regulatory compliance for cancer studies. They will also collaborate with investigators to facilitate participant recruitment, study visits, and the preparation of research materials.
$21 - $31 / HOUR
14 days ago
University of Virginia
The coordinator will manage study protocols, recruit and enroll participants, and obtain informed consent. Responsibilities also include collecting participant data and processing laboratory specimens within the Emergency Department and related units.
17 days ago
UVA Health
The coordinator will manage study protocols, recruit and enroll participants, and obtain informed consent. They are also responsible for collecting participant data and processing laboratory specimens within the Emergency Department and related units.
18 days ago
