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Weill Cornell Medical College
Overview
Oversees daily laboratory activities and coordinates investigative procedures under guidance. Responsibilities include designing experiments, analyzing results, and maintaining laboratory protocols and quality standards.
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Compensation
$31 - $39 / HOUR
Posted
10 days ago
University of Texas Medical Branch (UTMB)
The coordinator obtains human subject data according to study protocols and manages general administrative duties to support clinical research. Key tasks include recruiting participants, maintaining regulatory documentation, and processing laboratory specimens.
Salary not listed
16 days ago
The coordinator obtains human subject data according to study protocols and performs administrative duties to support clinical research. Key tasks include recruiting participants, managing regulatory documentation, and processing laboratory specimens.
University of Massachusetts Medical School
The Clinical Research Coordinator I is responsible for coordinating regulatory activities and managing data collection for research protocols. This includes obtaining consent from participants, scheduling visits, and ensuring compliance with study protocols.
$40,000 - $48,000
23 days ago
UT Health San Antonio
Provide technical assistance for research projects focusing on recurrent pregnancy loss in humans. Responsibilities include conducting scientific experiments, interpreting clinical data, and performing limited administrative laboratory duties.
29 days ago
Mount Sinai Health System
The coordinator is responsible for conducting clinical research studies, obtaining informed consent, and organizing study information. They also assist in preparing and submitting grant applications and IRB documentation.
1 month ago
Boys Town
The Research Assistant will support laboratory operations by performing data collection, equipment calibration, and subject recruitment for human or animal research studies. They are also responsible for maintaining detailed records, preparing test materials, and assisting in the construction and maintenance of laboratory electronic devices.
Franciscan Alliance, Inc.
The coordinator implements and completes clinical research protocols, including obtaining informed consent and performing protocol-specified procedures. They are responsible for recruiting subjects, maintaining documentation, and reporting adverse events to sponsors.
UCSF
The Assistant Clinical Research Coordinator will support a multi-disciplinary team in longitudinal studies on aging and cognitive decline. Responsibilities include managing study data, coordinating research activities, and interacting with human subjects under the supervision of the principal investigator.
$28 - $46 / HOUR
2 months ago
University of Colorado
This role involves supporting clinical research labs by assisting with and overseeing the day-to-day operations of clinical trials and studies. Key duties include managing subject eligibility, performing the informed consent process, collecting and processing patient specimens, and accurately collecting and analyzing research data.
$48,446 - $61,623 / YEAR
This role involves supporting clinical research labs by assisting with and overseeing the day-to-day operations of clinical trials and studies. Key duties include obtaining subject medical history, confirming eligibility, performing the informed consent process, collecting and processing specimens, and accurately analyzing research data.
PIH Health
The Clinical Research Coordinator manages and coordinates clinical research studies within a hospital, ensuring adherence to regulatory requirements and institutional policies. This role supports the day-to-day execution of clinical trials through participant recruitment, data collection, compliance monitoring, and regulatory documentation.
$27 - $45 / HOUR
Vanderbilt University Medical Center
The coordinator is responsible for managing the approval processes and execution of research protocols to maintain research integrity and compliance with all policies. Key duties include preparing IRB submissions, maintaining regulatory documents, participating in site visits, recording data accurately, and managing study specimens and budgets.
3 months ago
Jefferson Health Plans
The coordinator oversees the day-to-day activities of a clinical trial following GCP, performing research activities like database management, specimen processing, and clerical duties to support investigators in compiling clinical research data. Responsibilities also include recruiting, assisting with consenting subjects, conducting study visits, and maintaining required documentation.
Wayne State University
Essential functions include performing laboratory-based scientific techniques or clinical/population science research, designing experiments, recruiting participants, and ensuring compliance with all regulatory guidelines. The role also involves collecting, analyzing, and summarizing research data for presentations and publications, alongside maintaining laboratory areas and supplies.
The Research Assistant will perform laboratory-based scientific techniques or clinical/population science research, including designing and executing experiments and recruiting study participants. Essential duties also involve collecting, logging, evaluating, and analyzing research data, ensuring compliance with all guidelines, and assisting with documentation for presentations and publications.
