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DM CLINICAL RESEARCH GROUP
Overview
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.
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Compensation
Salary not listed
Posted
11 days ago
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The Principal Investigator will serve as the lead for multiple clinical trials (Phases I to IV), taking responsibility for clinical research conduct, quality assurance, and supervising sub-investigators. This role involves attending site initiation visits, sponsor monitoring visits, and evaluating study volunteer eligibility according to regulations.
3 months ago
