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IQVIANew
Overview
The Research Coordinator ensures effective conduct of clinical trials by advocating for patient safety, maintaining protocol integrity, and overseeing patient screening and study requirements. Responsibilities include adhering to federal/institutional regulations, managing informed consent processes, and coordinating all protocol-required patient events.
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Compensation
$43,400 - $108,200 / YEAR
Posted
New
University of Miami
The coordinator manages simple clinical research protocols, including participant screening, enrollment, and data collection. They perform clinical procedures such as phlebotomy and pulmonary assessments while ensuring regulatory compliance and maintaining study records.
Salary not listed
23 days ago
University of Rochester
Coordinates administrative and operational activities for human subject research, including participant recruitment, screening, and protocol adherence. Acts as a liaison between the Principal Investigator, sponsors, and the Institutional Review Board to ensure regulatory compliance and data accuracy.
$21 - $30 / HOUR
1 month ago
Coordinates administrative activities for multi-site clinical research studies, including participant recruitment and consent. Manages study visits, ensures regulatory compliance, and assists in disseminating research findings through publications.
CenExel
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
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
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
US Foot & Ankle Specialists
The Clinical Research Coordinator will independently manage and execute clinical trials, overseeing day-to-day study operations, regulatory compliance, patient coordination, and data management according to protocol and guidelines. Key duties include managing the full study lifecycle from start-up to closeout, ensuring compliance, and coordinating with investigators, sponsors, and the IRB.
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
This role provides direct support to Clinical Research Coordinators by ensuring adherence to all protocol and regulatory guidelines while managing patient charts and visit materials. Essential duties include timely data entry, resolving queries, assisting with participant assessments, and maintaining study supply inventory.
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.
$20 - $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.
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.
The Research Assistant I directly supports 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 for participant visits, conducting assessments like blood pressure and urine collection, and timely data entry and query resolution.
$19 - $20 / HOUR
Flourish Research
The Clinical Research Coordinator assists Investigators in executing clinical research trials according to protocols and regulations. Responsibilities include patient visits, documentation, informed consent, and maintaining communication with the study team.
$72,000 - $79,000 / YEAR
University of Colorado
The primary responsibility is serving as a Clinical Research Coordinator, overseeing day-to-day operations for multiple clinical trials and ensuring alignment with established protocols. Key duties include subject recruitment, executing informed consent, performing study procedures like phlebotomy, and managing data entry into CRFs.
$48,446 - $60,000 / YEAR
The primary responsibility is to serve as a Clinical Research Coordinator supporting various research activities, overseeing day-to-day operations for multiple clinical trials, and ensuring protocol alignment. Key duties include subject recruitment, informed consent execution, performing study procedures like phlebotomy, and managing data entry into CRFs.
This role involves providing direct support to Clinical Research Coordinators to achieve protocol-specific study goals while strictly adhering to all relevant guidelines and policies. Key duties include creating and maintaining patient charts, preparing participant visits, managing study supplies, and timely completion of data entry and query resolution for CRFs.
$20 - $22 / HOUR
The Medical Assistant 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, performing phlebotomy, conducting assessments like blood pressure and urine collection, and timely data entry.
$18 - $21 / HOUR
4 months ago
