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Duke Careers
Overview
Perform technical and clerical duties to support clinical research, including participant recruitment, data collection, and specimen processing. Ensure compliance with regulatory policies and assist in the preparation of IRB documentation and study reports.
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Compensation
$20 - $31 / HOUR
Posted
2 days ago
Vail Health Hospital
The Clinical Research Coordinator manages clinical trials by ensuring patient safety, regulatory compliance, and accurate data collection. They coordinate patient recruitment, maintain study documentation, and facilitate communication between investigators, sponsors, and clinical staff.
$32 - $44 / HOUR
8 days ago
OneOncology
The Clinical Research Coordinator independently manages study coordination, including patient screening, informed consent, and accurate data collection. They ensure compliance with FDA and IRB regulations while reporting study activity and accrual data to staff.
$70,000 - $80,000 / YEAR
23 days ago
University of Maryland Medical System
The role involves coordinating clinical research trials in radiation oncology, including protocol submission, patient recruitment, and data management. The coordinator acts as a liaison between sponsors, investigators, and review boards to ensure regulatory compliance and study integrity.
Salary not listed
24 days ago
Cedars-Sinai
Coordinates clinical research studies for kidney transplants, including patient screening, informed consent, and data collection. Ensures strict compliance with FDA, IRB, and GCP guidelines while managing study documentation and reporting.
$24 - $40 / HOUR
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
Hackensack Meridian Health
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials, ensuring compliant patient care and regulatory adherence. Responsibilities include recruiting patients, managing informed consent, monitoring patient progress, and acting as a liaison between investigators and sponsors.
$55,962 / YEAR
29 days ago
Johns Hopkins University
Oversee day-to-day activities of complex oncology clinical studies and ensure operational feasibility of study designs. Manage participant recruitment, data collection systems, and maintain compliance with all applicable regulations and protocols.
$41,300 - $72,300 / YEAR
1 month ago
American Oncology Network
Responsible for the clinical and administrative management of complex oncology research studies, including phase 1-3 trials. Key duties include coordinating patient care, ensuring regulatory compliance, and managing study data and budgets.
$26 - $45 / HOUR
The coordinator manages clinical study activities, including patient screening, informed consent, and data collection. They ensure strict compliance with FDA and IRB regulations while maintaining accurate source documentation and reporting study progress.
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
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.
$113,610 / YEAR
The Senior Research Nurse coordinates and implements clinical trials within the oncology research program, ensuring protocol compliance and subject safety. They manage project documentation, oversee data collection, and provide education to patients and staff throughout the research process.
$75,100 - $131,700 / YEAR