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Description: The Drug Safety Associate will be responsible for the review, evaluation and management of adverse event reports from FG-4592, FG-3019, and other clinical trials in accordance with FDA, EMEA, CFDA, other applicable health authorities and ICH guidelines and7/30/2014 San Francisco, CA Save This Job
Description: FibroGen seeks a Clinical Quality Assurance (CQA) Associate Director / Senior Manager to support the company?s Clinical Quality Assurance program. The incumbent will conduct and manage Good Clinical Practice (GCP) related quality audits (e.g., investigator site and6/30/2014 San Francisco, CA Save This Job