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IRONWOOD PHYSICIANS,P.C.New
Overview
Responsible for the timely submission and maintenance of accurate regulatory documents to pharmaceutical sponsors, IRBs, and contract research organizations. Oversees study initiation, monitoring, and closeout visits while ensuring compliance with federal regulations and international guidelines.
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Compensation
Salary not listed
Posted
New
DM CLINICAL RESEARCH GROUP
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.
12 days ago
