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Iterative Health
Overview
The Clinical Research Coordinator supports and facilitates daily clinical trial activities, including patient recruitment, screening, and protocol management. They are responsible for maintaining accurate study documentation, ensuring regulatory compliance, and communicating effectively with study sponsors and site staff.
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Compensation
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Posted
15 days ago
UT Southwestern Medical Center
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and patient safety monitoring according to protocol guidelines.
22 days ago
Coordinate a portfolio of high-complexity neurological surgery trials, including investigator-initiated and industry-funded studies. Manage regulatory compliance, subject recruitment, data collection, and the execution of study procedures according to protocol.
23 days ago
Children's Healthcare of Atlanta
Develops and implements research protocols while managing participant enrollment, data integrity, and specimen acquisition. Coordinates regulatory processes, including IRB submissions and financial tasks, to support principal investigators in endocrinology research.
Johns Hopkins University
The Peer Specialist supports research projects through data collection, organization, and administrative tasks. Additionally, they provide direct harm reduction services, mobile outreach, and health education at the SPARC center for marginalized populations.
$16 - $26 / HOUR
25 days ago
Coordinate and manage a portfolio of high-complexity clinical trials within the Department of Neurological Surgery. Responsibilities include managing regulatory documentation, recruiting participants, and ensuring compliance with FDA and University policies.
27 days ago
Coordinate and manage a portfolio of high-complexity clinical trials in Neurological Surgery, including investigator-initiated and industry-funded studies. Responsibilities include recruiting participants, managing regulatory documentation, and ensuring compliance with FDA and University policies.
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
28 days ago
The coordinator administratively manages clinical protocol implementation, ensuring adherence to study guidelines and validity of findings. Responsibilities include participant recruitment, consenting, data collection, and the processing and tracking of biospecimens.
$17 - $30 / HOUR
1 month ago
The coordinator will administratively manage clinical protocol implementation and ensure the logistical execution of study activities. Key duties include participant recruitment, consenting, data collection, and coordinating submissions to the Institutional Review Board.
The coordinator administratively manages clinical protocol implementation for neurology studies, ensuring adherence to protocols and validity of findings. Key duties include participant recruitment, consenting, data collection, and coordinating with the Institutional Review Board.
University of California, Irvine
The Assistant Clinical Research Coordinator supports cancer-related clinical trials by managing data, coordinating protocol requirements, and assisting the Principal Investigator with patient recruitment and screening. They also serve as a liaison between sponsors, regulatory agencies, and the research team to ensure compliance with institutional and federal policies.
$113,610 / YEAR
Arizona Liver Health
The Clinical Research Coordinator manages the conduct of clinical trials by implementing protocols, recruiting participants, and ensuring compliance with regulatory standards. They are responsible for collecting and recording research data, performing clinical assessments, and maintaining study documentation.
$28 - $36 / HOUR
The Research Program Coordinator manages daily logistical and operational activities for clinical research studies, including participant recruitment, enrollment, and data integrity. They also serve as a liaison between clinical staff, investigators, and community partners while ensuring adherence to study protocols and regulatory requirements.
The Clinical Research Coordinator will manage the logistical implementation of clinical protocols and ensure adherence to study activities. They will also provide administrative support for regulatory issues, including IRB submissions and participant recruitment.
Saint Louis University
The Clinical Research Nurse manages complex study protocols, including patient screening, enrollment, and the administration of investigational interventions. They act as a liaison between the research team, clinical partners, and regulatory bodies to ensure adherence to Good Clinical Practice standards.
The Clinical Research Nurse coordinates and oversees clinical research operations for assigned trials while ensuring compliant patient care. They act as a liaison between investigators and regulatory bodies, manage study documentation, and monitor patient progress throughout the clinical trial process.
$106,330 / YEAR
2 months ago
Prometrika LLC
The Clinical Trial Associate supports, coordinates, and implements clinical research projects under general supervision. Responsibilities include assisting with study start-up, maintaining study documentation, and ensuring compliance with clinical study standards.
$60,000 - $75,000 / YEAR
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, assisting personnel, managing participant recruitment and consenting, and handling data entry and IRB submissions.