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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
28 days ago
The Research Assistant I 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, conduct basic assessments, and facilitate communication between study stakeholders.
1 month ago
The Clinical Research Coordinator is responsible for managing all aspects of clinical trials, including patient involvement, data collection, and regulatory compliance. They also assist with site operations, vendor oversight, and the education of study participants regarding protocol expectations.
The Psychiatric Technician interacts directly with patients in clinical trials, observing behavior and assisting with daily living activities. They also support the clinical team by ensuring protocol adherence, facilitating group activities, and assisting with medication administration.
$19 - $23 / HOUR
The technician is responsible for conducting diagnostic testing, maintaining laboratory logs, and ensuring strict adherence to clinical research protocols and regulatory standards. They also assist in site preparation, sample management, and the organization of study supplies.
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
2 months ago
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
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
3 months ago
The Patient Care Technician assesses participants' psychosocial and case management needs, observes behavior changes, and assists subjects with ADLs, meals, laundry, and housekeeping while ensuring strict adherence to study protocols. Responsibilities also include coordinating discharge planning, managing necessary documentation, and developing relationships with external agencies to support participant services.
$20 - $21 / 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.
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
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.
4 months ago
