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4 C Medical Technologies
Overview
This role involves developing, coordinating, and administering the logistical aspects of clinical trials in compliance with GCP, GDP, and SOPs, acting as a key communication point between staff, sites, and vendors. Key duties include overseeing trial operations, managing site documentation, corresponding with study sites regarding subject progress and queries, and coordinating adverse event information.
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Compensation
$75,000 - $95,000 / YEAR
Posted
7 days ago
Headlands Research
Lead and oversee clinical trials ensuring compliance with protocols and ethical guidelines. Provide leadership and mentorship to site staff while overseeing subject safety and trial conduct compliance.
$130 - $160 / HOUR
10 days ago
UCSF
The coordinator executes and manages clinical research protocols, overseeing data collection, specimen management, and regulatory compliance. They act as an intermediary between departments and assist in the training and oversight of research staff.
$38 - $61 / HOUR
11 days ago
Wayne State University
Essential functions include performing laboratory-based scientific techniques or clinical/population science research, designing experiments, recruiting participants, and ensuring compliance with all regulatory guidelines. The role also involves collecting, analyzing, and summarizing research data for presentations and publications, alongside maintaining laboratory areas and supplies.
Salary not listed
3 months ago
