Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
University of Rochester
Overview
This role coordinates human subject research activities within the Department of Urology, focusing on screening, consenting subjects, maintaining documentation, and managing data collection according to research protocols. The specialist ensures research activities adhere to institutional policies, IRB requirements, and study protocols while coordinating with the Principal Investigator and other study team members.
Quick view →
Compensation
$21 - $30 / HOUR
Posted
8 days ago
Headlands Research
Support clinical trial execution by conducting patient recruitment through outbound calls and assisting with subject screening and enrollment. Collect vital signs and document study data in electronic systems while ensuring compliance with study protocols.
Salary not listed
9 days ago
OneOncology
This role involves assisting with various clinical research activities under mentorship, including screening potential subjects for eligibility against trial criteria and managing informed consent records. The coordinator will also be responsible for procuring, processing, and shipping biospecimens according to protocol and regulations.
2 months ago
US Foot & Ankle Specialists
The Clinical Research Coordinator manages and conducts clinical research projects, leading trial operations, collecting data, and ensuring strict adherence to Foot and Ankle Specialists of the Mid-Atlantic (FASMA) Standard Operating Procedures (SOPs). Key duties include acting as a liaison between investigators, sponsors, and regulatory bodies, maintaining all required study documentation, and overseeing subject enrollment and data entry.
4 months ago
