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Pharmacovigilance Associate â Cambridgeshire
Date Posted: Jan 11, 2012
Following your company induction and any training required you will have the following responsibilities: Key Responsibilities: F0D8;Case processing including data entry, review and assessment of SAE/AE reports from clinical trials and post marketing sources onto their global safety database (ARISg), in accordance with SOP (Standard operating procedures), F0D8;Assist in SAE reconciliation, F0D8;Utilise and maintain the global safety database, F0D8;Contribute to the on going enhancement of Drug Safety processes and SOPs...View full job description
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