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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, conducting basic assessments like blood pressure, and coordinating with study participants and vendors.
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Compensation
$18 - $22 / HOUR
Posted
24 days ago
The Research Assistant provides direct support to Clinical Research Coordinators by managing patient charts, preparing visit materials, and performing data entry. They also conduct basic clinical assessments and maintain study-specific supplies while adhering to strict regulatory guidelines.
Salary not listed
29 days ago
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and assisting with clinical assessments. They are also responsible for data entry, query resolution, and facilitating study monitoring visits while adhering to strict research protocols.
$20 - $21 / HOUR
1 month ago
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
$20 - $22 / HOUR
Profound Research
The Clinical Research Coordinator manages all clinical trial activities in compliance with study protocols, regulations, and company standards. They are responsible for subject recruitment, data collection, regulatory documentation, and mentoring staff to ensure high-quality clinical research operations.
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and ensuring accurate data entry. They also assist with participant visits, clerical tasks, and the facilitation of study monitoring visits.
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, preparing visit materials, and assisting with clinical assessments. They also handle data entry, inventory management, and facilitate study monitoring visits while ensuring strict adherence to protocol guidelines.
The Research Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, managing study supplies, and performing data entry. They also assist with participant assessments, scheduling, and the facilitation of study monitoring visits.
2 months ago
The Medical Assistant provides direct support to Clinical Research Coordinators by maintaining patient charts, preparing visit materials, and assisting with clinical assessments. They are also responsible for data entry, inventory management, and facilitating study monitoring visits.
$20 / 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 all Case Report Forms (CRFs).
$20 - $23 / HOUR
This role provides direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to all relevant guidelines and policies. Key duties involve creating and maintaining patient charts, managing study supplies, timely data entry and query resolution, and assisting with participant assessments and scheduling.
The Research Assistant I supports Clinical Research Coordinators by creating and maintaining patient charts, preparing for participant visits, and ensuring all necessary study materials are available and accurate. Key duties also involve timely data entry, query resolution for CRFs, conducting basic participant assessments, and assisting with monitoring visits.
$19 - $21 / 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.
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.
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. Essential duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely data entry and query resolution for CRFs.
$21 - $25 / 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 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
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 involve creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely completion of data entry and query resolution for CRFs.
This role provides direct support to Clinical Research Coordinators by ensuring strict adherence to ICH, GCP, protocol, and site guidelines while completing protocol-specific study goals. Essential duties include creating and maintaining patient charts, preparing participant visits, managing study supply inventory, and timely data entry and query resolution.
