Pharmacovigilance Specialist (12 Month Contract)
Mississauga, Canada, Canada, Canada Numéro du poste JR0126851 Catégorie Regulatory Monitoring, Compliance & Legal Date de publication Mar. 04, 2025McKesson, l’une des 10 premières entreprises du classement Fortune Global 500, touche à pratiquement tous les aspects des soins de santé et s’emploie à faire une réelle différence. Nous sommes reconnus pour notre capacité à offrir un savoir, des produits et des services qui rendent les soins de qualité plus accessibles et plus abordables. Chez nous, la santé, le bonheur et le bien-être de nos gens et des personnes que nous desservons sont prioritaires—et nous tiennent à cœur.
Ce que tu fais chez McKesson a de l’importance. Nous favorisons une culture où tu peux t’épanouir et avoir un impact, et où tu es encouragé à proposer de nouvelles idées. Ensemble, nous façonnons l’avenir de la santé pour nos patients, nos communautés et nos équipes. Si tu souhaites dès aujourd’hui contribuer à la santé de demain, nous aimerions avoir de tes nouvelles.
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.
Job Summary
The Bilingual Pharmacovigilance (PV) Specialist is an integral part of the pharmacovigilance team, and is responsible for the identification, collection, documentation, processing and reporting of adverse event data in compliance with Health Canada regulations and client specific requirements.
The Bilingual PV Specialist will ensure accurate and comprehensive data entry of adverse event information in a timely manner. They are also responsible for supporting the pharmacovigilance team in activities related to quality safety reviews, internal pharmacovigilance auditing, and deviation investigation & management.
Specific Responsibilities
- Management of adverse events from all relevant sources
- Ensure all adverse events are processed in a timely manner according to client requirements
- Demonstrate diligence in follow-up attempts to ensure all necessary information for case completeness
- Ensure adequate documentation and archiving of all drug safety information and source documentation
- The ability to accurately record and represent relevant information from medical and diagnostic reports and prepare concise narrative summaries of safety information
- The ability to work independently across multiple projects and work collaboratively with other team members and colleagues across disciplines
- The ability to follow established processes and the flexibility to adopt new practices and priorities as required
- Work with clients, as required, to ensure processes and strategies are maintained, internal and external timelines are met, potential issues are communicated, and resolution is achieved in a timely manner
- Support inspection readiness and audits as required
- Manage activities in specific projects as assigned
General Responsibilities
- Ability to prioritize and reprioritize work in a constantly changing environment
- Adhere to professional standards as stipulated by the relevant governing professional bodies
- Participate and assist in departmental continuous improvement activities related to process, quality, and training
- Assist with reviews of aggregate data to identify program trends and communicate these trends appropriately
- Maintain program data integrity through the quality review of program documentation, ensuring completeness and accuracy
- Perform other duties as assigned
Competencies
- Healthcare professional experience (licensed HCP in Canada) is required
- Bilingual in English and French is an asset
- Previous experience in pharmacovigilance activities an asset
- Proficiency in Microsoft Office programs (Word, Excel, Outlook)
- Attention to detail and excellent organizational skills
We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, please click here.
Notre échelle salariale de base pour ce poste
Our Base Pay Range for this position
$71,400 - $119,000McKesson est un employeur qui adhère aux principes d’égalité d’accès à l’emploi.
McKesson offre des possibilités d'emploi égales aux candidat·e·s et aux employés, et s'engage à créer un environnement diversifié et inclusif, sans distinction de race, de couleur, de religion, de sexe, d'orientation sexuelle, d'identité de genre, d'origine nationale, de statut de vétéran protégé, de handicap, d'âge ou d'informations génétiques. Pour en savoir davantage sur les politiques de McKesson à cet égard, veuillez consulter notre page sur l'égalité des chances en matière d'emploi.
McKesson is an Equal Opportunity Employer
McKesson provides equal employment opportunities to applicants and employees and is committed to a diverse and inclusive environment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age or genetic information. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.
Join us at McKesson!
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Avantages sociaux
Découvrez notre large éventail d'avantages sociaux en matière de santé, d'avantages financiers, de programmes de mieux-être et d'horaires de travail flexibles.
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Prêt·e pour la prochaine étape ? Nous vous guiderons tout au long du processus d'embauche.
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Améliorer les résultats en matière de santé pour tous : c'est le fondement de nos interactions avec nos clients, nos partenaires commerciaux et entre nous. Rencontrez l'équipe et découvrez notre mission.
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Notre culture est fondée sur la diversité des points de vue, et nous valorisons le parcours, l'expérience et les idées uniques de chaque personne.
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