Stage- Pharmacovigilance job opportunity at AstraZeneca.



DateMore Than 30 Days Ago bot
AstraZeneca Stage- Pharmacovigilance
Experience: General
Pattern: full-time
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loacation France - La Defense, France
loacation France - La De..........France

Contexte : AstraZeneca est un groupe biopharmaceutique international guidé par la science, axé sur la recherche, le développement, la production et la commercialisation de médicaments de prescription. Notre activité se concentre dans des domaines thérapeutiques majeurs : maladies cardiovasculaires et métaboliques, respiratoire, oncologie. Nous intervenons dans plus de 100 pays et nos médicaments innovants sont utilisés par des millions de patients à travers le monde. Votre mission : Au sein de la direction médicale de la filiale AstraZeneca France et sous la responsabilité du Directeur Pharmacovigilance et Information Médicale, vous participerez aux missions suivantes : Pharmacovigilance : Recueillir, valider et évaluer l'imputabilité des notifications des effets indésirables présumés survenus en France ; mettre en œuvre la procédure de traitement adéquate. Saisir les cas dans la base de données locale de pharmacovigilance. Enregistrer et déclarer les cas de pharmacovigilance aux autorités sanitaires dans les délais requis et dans le respect de la réglementation en vigueur (cas spontanés et essais cliniques). Veiller à l'archivage dans les dossiers de tout élément d'information sur les effets indésirables signalés. Participer à l'information médicale sur la sécurité de l'utilisation et la tolérance des spécialités pharmaceutiques auprès des professionnels de la santé. Prendre en charge les réclamations Qualité Produit liées à des cas de pharmacovigilance, en collaboration avec le service Assurance Qualité Produit. Assurer le suivi du bon usage des médicaments et participer aux Comités Bon Usage. Assurer la détection et la revue périodique des signaux. Rédiger la partie pharmacovigilance des dossiers de demande de remboursement. Assurer le suivi des modifications de l’information sur les produits. Rédiger la partie pharmacovigilance des protocoles d’études cliniques, des cahiers d’observation et des rapports d’études. Assurer le suivi de la tolérance dans le cadre des ATU et la rédaction des rapports périodiques. Assurer la veille bibliographique sur les revues françaises pour la détection de signalements de Pharmacovigilance. Date Posted 03-sept.-2025 Closing Date AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

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