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M3USA
Overview
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the Investigator with participant screening, maintaining documentation, collecting and entering data, and overseeing other research staff.
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Compensation
$30 - $40 / HOUR
Posted
16 days ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily activities of clinical trials under the guidance of site management and the Principal Investigator. Essential duties include assisting investigators with participant screening, maintaining documentation, mentoring staff, and ensuring all activities comply with research protocols and regulations.
Salary not listed
University Hospitals
The therapist performs pulmonary function tests and manages subject scheduling to support clinical research studies. Responsibilities include executing protocols such as DLCO and 6mwt, maintaining research logs, and collaborating with coordinators to align tests with patient visits.
23 days ago
Washington University in St. Louis
This role coordinates and implements research studies, managing data collection while ensuring continuity of patient care and protection of human subjects under the Principal Investigator's guidance. Responsibilities include providing direct patient care, administering study interventions and medications, processing specimens, and collaborating with multidisciplinary teams and sponsors.
$56,200 - $96,100 / YEAR
29 days ago
The Clinical Research Coordinator manages daily clinical trial activities and supports the Principal Investigator in the conduct of studies. Key duties include screening participants, maintaining documentation, and ensuring compliance with research protocols and laws.
1 month ago
The Clinical Research Coordinator manages, supports, facilitates, and coordinates the daily clinical trial activities under the guidance of site management and the Principal Investigator. Essential duties include assisting the investigator with participant screening, maintaining documentation, and ensuring all activities comply with the research protocol and regulations.
The Clinical Research Coordinator manages and coordinates daily clinical trial activities under the guidance of the Principal Investigator. They assist in screening participants, maintaining documentation, and ensuring compliance with research protocols.
Caris Life Sciences
Provide operational and regulatory support for sponsored and collaborative pharma studies, focusing on site onboarding and engagement. Manage study documentation, specimen tracking, and inventory while ensuring compliance with SOPs.
Coordinates and implements cardiology research studies, including data collection, patient screening, and enrollment. Manages protocol requirements, regulatory submissions to the IRB, and the administration of investigational products.
University of Chicago
The Clinical Research Coordinator I facilitates daily clinical research activities, including participant screening, enrollment, and data collection. They ensure study compliance with federal and institutional regulations while maintaining accurate documentation and coordinating patient schedules.
$50,000 - $65,000 / YEAR
HonorHealth
The coordinator facilitates regulatory affairs for clinical research, ensuring compliance with FDA, ICH, and IRB standards. They manage study protocols from startup through closure, including document preparation and regulatory correspondence.
The Clinical Trial Specialist provides operational and regulatory support for sponsored and collaborative studies, including site onboarding and IRB submission management. They are also responsible for maintaining study documentation, tracking clinical biospecimens, and ensuring compliance with Good Clinical Practice guidelines.
HUCKEYE HEALTH SERVICES LLC
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$48 / HOUR
2 months ago
The Clinical Research Coordinator manages complex clinical research trials in collaboration with physicians and stakeholders. They ensure full compliance with GCP, FDA regulations, and human subject protection standards throughout the study lifecycle.
$43 / HOUR
3 months ago
The Clinical Research Coordinator manages the end-to-end coordination and operational support of complex clinical research trials. They ensure all study activities comply with Good Clinical Practice, FDA regulations, and human subject protection standards.
4 months ago
The Clinical Research Coordinator manages complex clinical trials including drug, device, and biologic studies across all phases. They work closely with study physicians and stakeholders to ensure compliance with Good Clinical Practice and FDA regulations.
$50 / HOUR
