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DM CLINICAL RESEARCH GROUP
Overview
Responsible for compounding, dispensing, and managing Investigational Products (IP) according to sponsor-approved protocols. The role involves maintaining IP accountability records, ensuring blinding plan compliance, and coordinating with Principal Investigators and sponsors.
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Compensation
Salary not listed
Posted
11 days ago
The Clinical Research Coordinator II ensures quality research is conducted at investigative sites in compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines. Key duties include managing subject visits, handling data entry, and overseeing the reporting of adverse events.
The Clinical Research Coordinator II ensures quality research is conducted at investigative sites following sponsor protocols, FDA regulations, and ICH/GCP guidelines. Key duties include managing subject visits, handling data entry, and overseeing the reporting of adverse events.
23 days ago
