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IQVIA
Overview
The Research Coordinator ensures effective conduct of clinical trials by advocating for patient safety, maintaining protocol integrity, and overseeing patient screening and study requirements. Responsibilities include adhering to federal/institutional regulations, managing informed consent processes, and coordinating all protocol-required patient events.
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Compensation
$43,400 - $108,200 / YEAR
Posted
2 days ago
INNOVO RESEARCH INC
The Clinical Research Coordinator manages clinical research data, regulatory documents, and patient records while performing clinical procedures. They are responsible for recruiting participants, executing study visits, and ensuring adherence to protocols and GCP standards.
$42,241 - $50,000 / YEAR
18 days ago
Washington University in St. Louis
Coordinate clinical research studies focusing on Epilepsy and rare pediatric diseases, acting as a liaison between investigators, sponsoring agencies, and participants. Manage all phases of study protocols, including participant recruitment, enrollment, and regulatory compliance reporting.
$47,400 - $71,200 / YEAR
1 month ago
Alcanza Clinical Research
The Clinical Research Registered Nurse ensures the execution of assigned studies and performs clinical procedures in compliance with study protocols and regulations. Responsibilities include patient screening, consent, follow-up visits, and documentation.
Salary not listed
2 months ago
Tufts Medicine
This role assists the Principal Investigator in planning and implementing clinical research studies, primarily by managing participant recruitment, conducting eligibility assessments, and obtaining informed consent. Essential duties also involve completing follow-up activities, abstracting source documents, completing Case Report Forms, and ensuring data quality prior to entry.
$44,779 - $55,978 / YEAR
This role assists the Principal Investigator in planning and implementing clinical research studies, primarily by managing participant recruitment, conducting eligibility assessments, and obtaining informed consent. Essential duties also involve completing follow-up activities, abstracting source documents, completing Case Report Forms, and ensuring data quality and entry.
Dana-Farber Cancer Institute
The Clinical Research Coordinator supports the research team in conducting clinical trials, primarily focusing on primary data collection, patient information management, and ensuring timely trial assessments and sample collection per protocol. Responsibilities also include maintaining study compliance with all state, federal, and IRB requirements, and managing study documentation and regulatory submissions.
$48,100 - $54,400 / YEAR
3 months ago
