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University of Chicago
Overview
The Protocol Coordinator manages the development and implementation of clinical trial protocols, ensuring compliance with regulatory requirements. They act as a liaison between study teams and funding agencies, addressing issues that arise during the protocol development process.
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Compensation
$60,000 - $85,000 / YEAR
Posted
1 month ago
Cedars-Sinai
The Regulatory Coordinator prepares and submits clinical trial protocols and supporting documentation to various regulatory bodies and committees. They ensure ongoing compliance with federal and local regulations, including FDA and IRB requirements, while maintaining accurate research files.
$34 - $58 / HOUR
Mount Sinai Health System
This role involves testing, coding, modeling, and reporting on Hospital Billing and Professional Billing contracts for the Health System to ensure accuracy of terms and reimbursement structures. The individual will also facilitate the flow of contract data into the revenue cycle system.
$19 - $29 / HOUR
2 months ago
Temple University
This role involves coordinating active Phase I-IV clinical trials under the supervision of the Regulatory Manager, interacting with sponsors, PIs, and research staff in the Thoracic Medicine & Surgery department. Responsibilities include maintaining regulatory compliance monitoring, preparing and processing all documentation through the IRB, and organizing regulatory affairs documentation.
$50,000 - $55,000 / YEAR
3 months ago
This role coordinates active Phase I-IV clinical trials under the Regulatory Manager, interacting with sponsors, PIs, and research staff in the Thoracic Medicine & Surgery department. Responsibilities include maintaining regulatory compliance monitoring, preparing IRB documentation, organizing regulatory files, and supporting quality assurance activities.
