Job Description
This position will be located in Spain; it is required to live in Spain and have a work permit.
Por favor, asegúrese de leer atentamente los siguientes detalles antes de enviar cualquier solicitud.
Job Overview
Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE submissions to CVM, pharmacovigilance SOPs, and Signal Management responsibilities.
Responsibilities
- Good understanding of the ADE reporting regulations (US and EU) and of product trending standards.
- Collaborate with signal management team regarding validation activities for assigned products (including signal detection) to comply with FDA/USDA/EU expectations and to better understand the safety and efficacy profiles of Zoetis products post‑marketing.
- Prepare trending repor...
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