Regulatory Research Assistant - (Clinical Research)
Riverside, CA, USAFull-timePosted Sep 1, 2026
Job description
Assist the Regulatory Specialists/Manager in maintaining clinical trial documents for submission to regulatory agencies in accordance to site SOPs, ICH, GCP, and FDA guidelines.
SOPs (Standard Operating Procedures) ICH (International Council for Harmonization) GCP (Good Clinical Practices) FDA (Food and Drug Administration)
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