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Ann & Robert H. Lurie Children's Hospital of Chicago
Overview
This role coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing documents, managing study conduct across departments, and overseeing all aspects of clinical research visits. Responsibilities also include managing participant engagement, collecting specimens, recording data, assisting with financial aspects, and participating in investigator meetings.
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Compensation
$49,920 - $81,619 / YEAR
Posted
7 days ago
Coordinates clinical research activities including regulatory compliance, IRB submissions, and the management of study documents. Oversees participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
14 days ago
Lurie Children's Hospital
Coordinates clinical research activities including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing while overseeing study supplies and financial invoicing.
15 days ago
Washington University in St. Louis
Assists the Principal Investigator in coordinating clinical research studies, ensuring regulatory compliance and IRB support. Manages project infrastructure, including budget oversight, data management via REDCap, and participant coordination.
$23 - $34 / HOUR
1 month ago
Coordinates clinical research activities, including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
Coordinates clinical research activities including regulatory compliance, IRB submissions, and the management of study documents. Manages participant engagement, specimen collection, and data processing to ensure protocol adherence and accuracy.
