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CenExel
Overview
Coordinate all aspects of patient involvement in clinical trials while adhering to ICH, GCP, and company guidelines. Perform safety and efficacy assessments, document adverse events, and manage regulatory duties to ensure study compliance.
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Compensation
$26 - $27 / HOUR
Posted
1 month ago
The coordinator is responsible for managing all phases of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines, from initiation through completion. This includes organizing research information, monitoring subjects, reporting adverse events, performing safety assessments, and assisting the Clinical Trial Manager with various operational aspects.
$30 - $38 / HOUR
3 months ago
The coordinator is responsible for managing all facets of clinical trials, ensuring strict adherence to ICH, GCP, protocol, and company guidelines from initiation through completion. This includes coordinating patient involvement, organizing research information, monitoring data quality, performing safety assessments, and assisting the Clinical Trial Manager with various oversight duties.
Salary not listed
4 months ago
The coordinator is responsible for managing all phases of clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. This includes organizing research information, monitoring subjects, performing safety assessments, and handling administrative and regulatory duties.
5 months ago
