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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 sourcesEnsure all adverse events are processed in a timely manner according to client requirementsDemonstrate diligence in follow-up attempts to ensure all necessary information for case completenessEnsure adequate documentation and archiving of all drug safety information and source documentationThe ability to accurately record and represent relevant information from medical and diagnostic reports and prepare concise narrative summaries of safety informationThe ability to work independently across multiple projects and work collaboratively with other team members and colleagues across disciplinesThe ability to follow established processes and the flexibility to adopt new practices and priorities as requiredWork 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 mannerSupport inspection readiness and audits as requiredManage activities in specific projects as assigned

General Responsibilities

Ability to prioritize and reprioritize work in a constantly changing environmentAdhere to professional standards as stipulated by the relevant governing professional bodiesParticipate and assist in departmental continuous improvement activities related to process, quality, and trainingAssist with reviews of aggregate data to identify program trends and communicate these trends appropriatelyMaintain program data integrity through the quality review of program documentation, ensuring completeness and accuracyPerform other duties as assigned

Competencies

Healthcare professional experience (licensed HCP in Canada)Bilingual in English and French is requiredPrevious experience in pharmacovigilance activities an assetProficiency 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.

Our Base Pay Range for this position

$71,400 - $119,000

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.

 

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