What your responsibilities will be
Cualquier información adicional que necesite para este trabajo se encuentra en el texto a continuación. Asegúrese de leerla detenidamente y luego envíe su solicitud.
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* You will provide operational support for global pharmacovigilance activities of Grifols marketed products
* You will ensure pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines
* You will be responsible for data review, compilation and analysis including management of the integrated safety database
* You will manage Adverse Events including activities such as processing adverse event case reports and conducts follow-up
* You will notify regulatory xhfqzwm agencies and business partners accordingly;
responds to requests from regulatory agencies
* You will draft and review periodic safety update reports
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