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Overview
The role focuses on the operational execution of clinical trials, including participant coordination, visit preparation, and specimen collection. Responsibilities also include entering study data into EDC systems and maintaining accurate source documentation.
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Compensation
$45,000 - $55,000 / YEAR
Posted
18 days ago
University of Chicago
The CRCII manages all aspects of clinical trials, including subject screening, enrollment, and data collection from start-up to close-out. They partner with the Principal Investigator to expand amyloid research and ensure strict adherence to federal regulations and institutional policies.
$60,000 - $75,000 / YEAR
24 days ago
Valley Health System
The Research Fellow will participate in advanced cardiovascular research, contributing to ongoing studies and developing independent projects. Responsibilities include study design, data analysis, manuscript preparation, and professional presentation of findings.
$80,340 / YEAR
27 days ago
The IMA Group
Coordinate clinical trials according to protocols and SOPs while maintaining accurate ALCOA documentation. Communicate with sponsors, CROs, and IRBs to ensure study data integrity and report adverse events.
$24 - $32 / HOUR
1 month ago
