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Research Assistant - Regulatory (Clinical Research)
Anaheim, CA, United StatesPosted Yesterday
Full-timeremote
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)