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University of Texas Medical Branch (UTMB)
Overview
The coordinator obtains human subject data according to study protocols and performs administrative duties to support clinical research. Key tasks include recruiting participants, managing regulatory documentation, and processing laboratory specimens.
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Compensation
Salary not listed
Posted
16 days ago
Care Access
The Clinical Research Coordinator II is responsible for screening, enrolling, and monitoring study subjects while ensuring strict adherence to protocol and regulatory compliance. They also manage patient coordination, perform clinical procedures, and maintain accurate study documentation.
$60,000 - $90,000 / YEAR
20 days ago
Hoag
The Clinical Research Coordinator II manages all facets of clinical research trials, including planning, implementation, and closure, ensuring smooth and accurate processes in cooperation with physicians and sponsors. Responsibilities include protocol review, obtaining informed consent, managing study documentation, data collection, sample processing according to IATA standards, and adverse event reporting.
$37 - $57 / HOUR
1 month ago
Allina Health
This role involves coordinating high-quality care for patients in clinical research studies by ensuring standards are met, educating participants, and collaborating across disciplines to support safe and effective study outcomes. Key duties include ensuring patient care aligns with the research protocol, performing safety monitoring, conducting patient evaluations, and assisting the investigator with protocol-specific tasks like dose modifications.
$37 - $51 / HOUR
Arizona Center for Cancer Care
The Clinical Research Assistant provides essential administrative and operational support for clinical research studies, focusing on document management, regulatory submissions, and scheduling under the supervision of the clinical program manager. This role involves assisting CRCs and investigators by ensuring study documentation is accurate, organized, and compliant with regulatory standards to facilitate efficient trial conduct.
2 months ago
The Clinical Research Coordinator III is responsible for managing all aspects of complex clinical research trials, including drug, device, and biologic studies, while collaborating with physicians and stakeholders. Key duties involve conducting protocol review, administering informed consent, recruiting subjects, ensuring accurate data collection, completing CRFs, and overseeing adverse event reporting and subject follow-up.
$39 - $59 / HOUR
Pharmaron
The Clinical Research Pharmacy Technician supports clinical research by managing the receipt, preparation, dispensing, storage, and accountability of investigational and non-investigational products under pharmacist supervision. Key duties include maintaining 100% product accountability, performing sterile and non-sterile compounding according to USP guidelines, and preparing necessary study documentation.
$25 - $29 / HOUR
