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University of Miami
Overview
The Clinical Research Coordinator 2 assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role involves day-to-day operations of clinical research protocol implementation and ensuring participant safety and adherence to approved protocols.
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Compensation
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Posted
12 days ago
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to guidelines. This role involves ensuring participant safety, adherence to protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies, managing day-to-day operations from initiation to close-out according to regulatory guidelines. This role involves ensuring participant safety, adhering to approved protocols, handling administrative tasks, facilitating information flow, and coordinating study activities and personnel.
The Clinical Research Coordinator 2 manages the day-to-day operations of clinical research protocols from initiation to close-out. Key duties include participant recruitment, data collection, specimen processing, and ensuring adherence to regulatory and sponsor guidelines.
The Clinical Research Coordinator 2 assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role involves day-to-day operations of clinical research protocol implementation and study coordination duties from protocol initiation to study close-out.
The Clinical Research Coordinator 2 assists in planning, coordinating, implementing, monitoring, and evaluating clinical research studies. This role includes participant recruitment, data collection, and ensuring adherence to protocols.
16 days ago
Johns Hopkins University
The specialist manages regulatory maintenance for oncology clinical trials, including IRB submissions and internal quality control. They also support program operations, train research staff, and facilitate compliance with institutional and federal research guidelines.
$48,000 - $84,100 / YEAR
1 month ago
Forward Health LLC
The Clinical Research Coordinator manages and executes clinical trials at the site level, ensuring compliance with study protocols and regulatory guidelines. They serve as the primary liaison between the Principal Investigator, study participants, and sponsors while overseeing subject recruitment, data management, and safety monitoring.
$17 - $35 / HOUR
Washington University in St. Louis
This role assists investigators by coordinating complex clinical research studies, potentially managing multiple studies simultaneously, and acting as a liaison between various stakeholders to ensure compliance with all required regulations and study protocols. Responsibilities include implementing and managing all study phases, establishing record-keeping systems, analyzing adverse events, and preparing progress reports and presentations.
$52,600 - $78,900 / YEAR
2 months ago
Temple University Health System
The Clinical Research Nurse will coordinate and facilitate clinical research protocols, ensuring participant recruitment, protocol compliance, and data quality. They will work closely with the clinical research team to develop tools for monitoring trial accrual and manage study activation and protocol amendments.
4 months ago
Florida Digestive Health Specialists LLP
The primary duties involve screening, enrolling, and following study subjects while ensuring strict adherence to protocol and regulatory compliance, often managing a greater study workload and increased interaction with Sponsors and CROs.
$61,000 - $68,000 / YEAR
5 months ago
