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CenExel
Overview
The Clinical Research Coordinator II manages patient involvement and clinical trial activities while ensuring strict adherence to ICH, GCP, and protocol guidelines. They also assist with data reporting, safety assessments, and provide support to the Clinical Trial Manager in site operations.
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Compensation
Salary not listed
Posted
1 month ago
The role is responsible for assisting in coordinating clinical trials while strictly adhering to ICH, GCP, protocol, and company guidelines, managing all aspects of patient involvement from initiation to completion. Duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments as required.
$30 - $33 / HOUR
2 months ago
The role is responsible for assisting in coordinating all aspects of clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety/efficacy assessments per protocol.
$28 - $35 / HOUR
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 subjects, reporting adverse events, and performing required safety and efficacy assessments.
3 months ago
The coordinator assists in managing all aspects of patient involvement in clinical trials from initiation to completion, ensuring strict adherence to ICH, GCP, protocol, and company guidelines. Key duties include organizing research information, observing subjects, scheduling data collection, documenting adverse events, and performing safety and efficacy assessments per protocol.
$29 - $33 / HOUR
4 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.
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
