Spécialiste en Pharmacovigilance/pharmacovigilance

6 months ago

Mississauga, Canada McKesson Full time

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care. What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.

McKesson touche la vie des patients en œuvrant dans pratiquement tous les secteurs des soins de santé dans le but d’améliorer la santé en général. Chez McKesson Canada, nous créons un impact dans la vie de 12 millions de Canadiens, chaque jour. Nous distribuons plus de 35 000 produits à partir de 12 centres de distribution à 6 300 pharmacies de détail, 1 350 hôpitaux, centres de santé longue durée, cliniques et établissements de santé partout au Canada. Toutefois, nous sommes beaucoup plus qu'une entreprise de distribution. Nous avons automatisé 2 500 pharmacies de détail et distribuons annuellement plus de 100 millions de doses de médicaments grâce à nos solutions d'automatisation. Les fabricants, les fournisseurs de soins de santé et les patients comptent sur nous pour une gamme complète de services qui contribuent à la qualité et l'intégrité des soins de santé pour le bénéfice de tous.

Chez McKesson, vous participerez à la création de produits et de solutions qui contribuent à la réalisation de la mission de l’entreprise, soit améliorer la qualité de vie et faire progresser les soins de santé. Travailler ici représente une occasion d’édifier une industrie qui est vitale pour nous tous.

**Résumé des fonctions**

Membre essentiel de l’équipe de pharmacovigilance, le ou la spécialiste en sécurité des médicaments est responsable de l’identification, de la collecte, de la documentation et du traitement des données sur les effets indésirables, ainsi que de la production de rapports connexes, conformément aux règles de Santé Canada et aux exigences spécifiques des clients. À ce poste, vous assurerez l’entrée de données exactes et complètes sur les effets indésirables, en temps opportun. Vous appuierez aussi l’équipe de pharmacovigilance dans les activités liées à l’évaluation de la qualité et de la sécurité, aux audits internes de pharmacovigilance, à la gestion des écarts et aux enquêtes connexes.

**Partie A - Responsabilités spécifiques**
- Gérer les données sur les effets indésirables de toutes les sources pertinentes
- Veiller à ce que les effets indésirables soient traités en temps opportun, conformément aux exigences du client
- Faire preuve de diligence dans les tentatives de suivi afin d’obtenir tous les renseignements requis pour le dossier
- Assurer la documentation et l’archivage adéquats de tous les renseignements sur la sécurité des médicaments et de la documentation source
- Consigner et présenter de façon exacte les renseignements pertinents tirés de rapports médicaux et rapports de diagnostic et préparer des sommaires des renseignements relatifs à la sécurité
- Travailler de façon indépendante sur de multiples projets et collaborer avec d’autres membres de l’équipe, ainsi que des collègues d’autres disciplines
- Suivre les processus établis et adopter de nouvelles pratiques et priorités au besoin
- Collaborer avec les clients, s’il y a lieu, afin de maintenir les processus et stratégies, de respecter les échéances internes et externes, de signaler les problèmes potentiels et de parvenir à une résolution rapidement
- Appuyer la préparation aux inspections et audits
- Gérer les activités de projets spécifiques qui lui sont confiés

**Partie B - Responsabilités générales**
- En mesure d’établir et de revoir la priorité des tâches dans un environnement en constante évolution
- Se conformer aux normes professionnelles stipulées par les organes directeurs pertinents
- Participer aux activités d’amélioration continue du service concernant les processus, la qualité et la formation
- Contribuer à l’examen des données agrégées pour repérer les tendances du programme et les communiquer aux personnes appropriées
- Maintenir l’intégrité des données du programme par un examen de la qualité de la documentation pour en assurer l’exactitude et l’exhaustivité
- Assumer d’autres fonctions au besoin

**Partie C - Compétences**
- Au moins 4 années d’expérience professionnelle en santé (professionnel de la santé agréé)
- La maîtrise du français
- Une expérience antérieure dans les activités de pharmacovigilance constitue un atout
- La maîtrise des programmes de la suite logicielle Microsoft Office (Word, Excel, Outlook)
- Un souc

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