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Avera Health
Overview
Coordinates and implements research study protocols, including participant recruitment, screening, and data collection. Manages laboratory specimens and ensures compliance with FDA regulations and Good Clinical Practices.
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Compensation
$22 - $37 / HOUR
Posted
4 days ago
Baptist Health System, Inc.
Conduct all aspects of clinical trials while ensuring compliance with local and federal regulations. Maintain Good Clinical Practice (GCP) standards to ensure subject safety and the validity of study data.
Salary not listed
8 days ago
Penn State University
The Human Research Technologist executes research protocols for clinical trials in Urology, focusing on participant recruitment and data collection. The role involves managing study visits, handling regulatory IRB submissions, and coordinating with principal investigators and sponsors.
$46,400 - $67,300 / YEAR
1 month ago
UCSF
The Clinical Research Coordinator will manage and coordinate clinical research protocols, ensuring compliance with UCSF and regulatory agency policies. Responsibilities include data collection, participant enrollment, database management, and overseeing study operations under the direction of the Principal Investigator.
$34 - $55 / HOUR
2 months ago
The Clinical Research Coordinator will manage and execute research protocols, oversee data integrity, and coordinate study operations under the guidance of the Principal Investigator. They will also act as an intermediary between departments, maintain regulatory documentation, and assist in the training of research staff.
The technologist will be accountable for all overnight sleep research recordings, including consecutive night studies for clinical trials, and will monitor and track research study files to ensure data quality control. Responsibilities also include performing Polysomnograms (PSGs), collecting Actigraphy data, maintaining lab equipment, and analyzing biological samples.