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NYU Langone Health
Overview
The Clinical Research Coordinator coordinates Endocrine clinical research studies from planning to completion, ensuring compliance with study protocols. Responsibilities include scheduling participants, preparing for study visits, and acting as the primary contact for bio-specimen collections.
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Compensation
$70,482 - $75,000 / YEAR
Posted
21 days ago
University of Chicago
The Clinical Research Coordinator 2 participates in the coordination and conduct of complex clinical research studies, ensuring compliance with regulations. They prepare and assist with research documentation and act as a liaison with various departments.
$60,000 - $75,000 / YEAR
1 month ago
IVF Florida
The coordinator supports clinical research studies from startup to closeout, managing regulatory submissions and sponsor communications. They provide high-quality patient care, conduct study visits, and ensure accurate data reporting and regulatory compliance.
Salary not listed
Arizona Center for Cancer Care
The Clinical Research Assistant provides essential administrative and operational support for clinical research studies, focusing on document management, regulatory submissions, and scheduling under the supervision of the clinical program manager. This role involves assisting CRCs and investigators by ensuring study documentation is accurate, organized, and compliant with regulatory standards to facilitate efficient trial conduct.
2 months ago
UCSF
The Clinical Research Coordinator independently manages and coordinates research protocols, ensuring regulatory compliance and data quality. Responsibilities include overseeing multiple clinical studies, supporting IRB submissions, and coordinating staff activities while adhering to institutional policies.
Johns Hopkins University
This role involves the administrative coordination of research protocol implementation, ensuring efficient logistical execution of study activities and providing administrative support for all related matters. Key duties include coordinating study activities to maintain finding validity, developing operational plans with senior staff, and overseeing data collection and record management.
$17 - $30 / HOUR
Jefferson Health Plans
The coordinator oversees the daily activities of a clinical trial following Good Clinical Research Practice (GCP), performing research activities like database management, specimen processing, and clerical duties to support investigators in compiling clinical research data. Responsibilities also include recruiting subjects, conducting study visits, maintaining documentation, and reporting patient responses or adverse effects to the Principal Investigator.
The coordinator will administratively manage the implementation of a clinical research protocol, ensuring efficient logistical execution and providing administrative support for regulatory matters. Key duties include coordinating all study activities to maintain protocol adherence and data validity, managing participant scheduling, and overseeing recruitment strategies.
3 months ago
University of Washington
This role involves acting as the initial point of contact for new clinical trial referrals, independently obtaining medical records for screening, and triaging patients for potential studies within the Cancer Vaccine Institute. Responsibilities also include explaining trial aspects to participants, managing data capture systems, documenting adverse events, and tracking study visits according to protocol.
$60,000 - $70,800 / YEAR
University of New Mexico
The Research Scientist will oversee retinal organoid maintenance and experiments, decode microglia associated inflammation gene regulatory networks, and assist in various co-culture and single-cell multi-omics experiments. They will also communicate research findings and contribute to grant preparation and support trainees in ongoing research projects.
$3,803 - $5,098 / MONTH
4 months ago
