CLINICAL DRUG SAFETY OFFICER

Sobre este empleo

What your responsibilities will be You will participate in the safety data collection, review, processing, evaluation, analysis and compilation You will process adverse event case reports (mainly Serious Adverse Events from clinical trials) and conduct follow-up, including definition of submissions to ensure compliance with regulatory agencies timelines for individual case reports You will provide technical oversight and be the pharmacovigilance representative for clinical studies You will be Subject Matter Expert for documents pertaining to clinical studies You will contribute to ensure compliance of pharmacovigilance activities with concerned departments such as clinical team or business partners You will conduct clinical pharmacovigilance activities such as development of safety…

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Salarios en España

Basado en 985 ofertas que indican el salario.

Estimado a partir del salario anunciado en nuestras fuentes: cifras brutas anuales orientativas, no una oferta.

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