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CenExel
Overview
Provides direct support to Clinical Research Coordinators by maintaining patient charts and preparing visit materials. Responsible for data entry, query resolution, and assisting with clinical assessments like blood pressure and urine collection.
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Compensation
$20 - $23 / HOUR
Posted
1 month ago
The Research Assistant II provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, conducting specific assessments, and timely completion of data entry and query resolution for CRFs.
Salary not listed
2 months ago
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties involve creating and maintaining patient charts, preparing for participant visits, timely data entry, and assisting coordinators with various assessments and clerical tasks.
3 months ago
Dana-Farber Cancer Institute
The Clinical Research Coordinator supports the research team in conducting clinical trials, primarily focusing on primary data collection, patient information management, and ensuring timely trial assessments and sample collection per protocol. Responsibilities also include maintaining study compliance with all state, federal, and IRB requirements, and managing study documentation and regulatory submissions.
$48,100 - $54,400 / YEAR
The Research Assistant I supports Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, conducting basic assessments, and timely completion of data entry and query resolution.
$19 - $22 / HOUR
This role provides direct support to Clinical Research Coordinators in achieving protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
$20 - $21 / HOUR
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to ICH, GCP, protocol, and site guidelines. Key duties include creating and maintaining patient charts, managing study supply inventory, and timely completion of data entry and query resolution for all CRFs.
$20 - $22 / HOUR
4 months ago
