Clinical Trials Coordinator & Compliance Specialist
Medix™
Medix seeks a Clinical Research Coordinator to assist with coordinating patient involvement from study initiation to completion. You will organize research information, observe subjects, collect data, and support data analysis and reporting. You will document adverse events, deviations, and other issues, maintain quality and compliance, and support regulatory duties. You will engage in protocol development, ensure sponsor communications, educate participants, and conduct safety assessments as #J-18808-Ljbffr Medix™
Vacancy posted 3 days ago
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