What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.
Enable to save this job to your wishlist - DATABASE DEVELOPER Enable to save this job to your wishlist - COUNTRY - Ukraine - FORMAT - Remote - JOB POSTED - 0 day(s) ago Svitla Systems Inc.