Find clinical, allied health, care team, and healthcare operations openings using one smart search field across cities, regions, and employers.
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.
Quick view →
Compensation
$18 - $22 / HOUR
Posted
24 days ago
The Clinical Research RN I oversees daily clinical study activities and serves as a liaison between the investigative site and the sponsor. Responsibilities include providing nursing care to participants, executing research protocols, and ensuring ethical documentation of all study data.
Salary not listed
28 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.
29 days ago
The Clinical Research RN I oversees daily clinical study activities and serves as a liaison between the investigative site and the Sponsor. Responsibilities include providing nursing care to participants, executing protocols, and ensuring ethical documentation of all research data.
$34 - $43 / HOUR
1 month ago
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.
$26 - $27 / HOUR
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
