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Description We're looking for a Drug Safety Associate , working in Biotechnology/Medical Devices industry in 350 DNA Way, South San Francisco, California, 94080, United States . Responsibilities: Establishes work priorities and direction independently with minimal input from Manager. Collects, documents, and processes adverse event (AE) reports from clinical trials and post-marketing sources in accordance with company Standard Operating Procedures (SOPs) and work practices to ensure and maintain regulatory compliance. Prepares clinical narrative summaries independently for AE reports from clinical studies and spontaneous post-marketing reports and formulates follow-up information requests. #J-18808-Ljbffr
