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University of Iowa
Overview
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
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Compensation
Salary not listed
Posted
3 days ago
Provide direct nursing care and administer investigational treatments for Phase I-IV clinical trials. Collaborate with medical staff to ensure participant safety and strict adherence to research protocols.
5 days ago
Georgetown University
Manage and coordinate a subset of clinical trials focusing on neuroimmunology and neuromuscular diseases, ensuring strict protocol adherence during patient visits. Responsible for regulatory maintenance, accurate data entry in OnCore/CTMS, and maintaining constant communication with patients and sponsors.
$44,022 - $73,407 / YEAR
15 days ago
Benaroya Research Institute
Provide administrative and operational support for cancer clinical trials, including regulatory maintenance and participant scheduling. Perform clinical procedures such as blood draws and vitals while managing study databases and supplies.
$24 - $34 / HOUR
16 days ago
Cleveland Clinic
Coordinate the implementation of human subject research projects while providing comprehensive nursing care to adult and pediatric patients. Responsibilities include administering study treatments, collecting clinical data, and ensuring adherence to research protocols and regulatory standards.
17 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
1 month ago
Carilion Clinic
The coordinator assists with administrative activities for industry, grant, or internally funded research studies while ensuring compliance with institutional and governing policies. Key duties include recruiting participants, obtaining informed consent, collecting data, and managing regulatory documentation for the IRB and FDA.
CenExel
This role involves advocating for research participants by addressing their psychosocial needs and assisting with retention during clinical trials, which includes performing phlebotomy and managing case needs.
$18 - $19 / HOUR
4 months ago
