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Orlando HealthNew
Overview
Develop and implement administrative strategies to manage clinical trials and coordinate large-scale research studies. Responsibilities include assessing patient eligibility, monitoring adverse reactions, and ensuring adherence to FDA and protocol guidelines.
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Compensation
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Cedars-Sinai
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and data collection. They ensure compliance with federal and local regulations while maintaining accurate source documents and reporting study progress.
$27 - $42 / HOUR
7 days ago
The US Oncology Network
The coordinator screens patients for protocol eligibility, manages the informed consent process, and coordinates patient care in compliance with research protocols. They are also responsible for accurate data collection, regulatory documentation, and collaborating with physicians to monitor adverse events.
17 days ago
ThedaCare
The Clinical Research Specialist coordinates clinical trials by screening patients for eligibility and managing the informed consent process. They are responsible for accurate data collection, maintaining source documents, and ensuring compliance with federal and institutional regulations.
26 days ago
The coordinator independently manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure strict compliance with FDA and IRB regulations while reporting study progress and accrual data to staff.
$28 - $48 / HOUR
1 month ago
The coordinator manages clinical study activities, including patient screening, informed consent, and accurate data collection. They ensure compliance with FDA and IRB regulations while reporting study progress and accrual data.
$24 - $40 / HOUR
The Clinical Research Coordinator manages study protocols, including patient screening, informed consent, and data collection. They ensure compliance with FDA and IRB regulations while maintaining accurate source documentation and reporting study progress.
The Clinical Research Coordinator screens and enrolls patients in clinical trials while ensuring strict compliance with study protocols and regulatory standards. They also collaborate with physicians to monitor patient conditions, manage investigational drugs, and maintain accurate research documentation.
HealthPartners
The Oncology Research Nurse independently manages patient care and conducts research by screening patients for protocol eligibility and coordinating care in compliance with study requirements. They also collaborate with physicians to monitor patient conditions, manage adverse events, and ensure accurate data collection and documentation.
$34 - $51 / HOUR
The Clinical Research Coordinator II independently manages study coordination, including screening patients for eligibility, presenting trial concepts, and handling the informed consent process. Responsibilities also include accurate and timely data collection, documentation, entry, reporting, and ensuring compliance with federal and local agencies like the FDA and IRB.
2 months ago
OneOncology
The Clinical Research Coordinator manages study protocols, including patient screening, informed consent, and accurate data documentation on Case Report Forms. They also ensure compliance with FDA and IRB regulations while coordinating research activities and reporting study progress to the research team.
$70,304 - $75,000 / YEAR
The coordinator screens patients for eligibility, presents trial details, manages informed consent, and coordinates patient care according to protocol requirements, which may include drug disbursement and patient teaching. Responsibilities also involve meticulous documentation of patient condition changes, adverse events, and study drug response in collaboration with the physician.
4 months ago
