Bilingual Pharmacovigilance Specialist (Apply in minutes)

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• Job Summary
• The Bilingual Pharmacovigilance (PV) Specialist is an integral part of thepharmacovigilance team, and is responsible for the identification, collection,documentation, processing and reporting of adverse event data in compliancewith Health Canada regulations and client specific requirements. The Bilingual PV Specialist will ensure accurate and comprehensive data entryof adverse event information in a timely manner. They are also responsible forsupporting the pharmacovigilance team in activities related to quality safetyreviews, 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)
• Bilingual in English and French is required
• Previous experience in pharmacovigilance activities an asset
• Proficiency in Microsoft Office programs (Word, Excel, Outlook)
• Attention to detail and excellent organizational skillsWe are proud to offer a competitive compensation package at McKesson as partof our Total Rewards. This is determined by several factors, includingperformance, experience and skills, equity, regular job market evaluations,and geographical markets. The pay range shown below is aligned with McKessonspay philosophy, and pay will always be compliant with any applicableregulations. In addition to base pay, other compensation, such as an annualbonus or long-term incentive opportunities may be offered. For moreinformation regarding benefits at McKesson, please [clickhere.](https : careers.mckesson.comenbenefits)
• 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 employeesand is committed to a diverse and inclusive environment without regard torace, color, religion, sex, sexual orientation, gender identity, nationalorigin, protected veteran status, disability, age or genetic information. Foradditional information on McKesson’s full Equal Employment Opportunitypolicies, visit our [Equal EmploymentOpportunity](https : www.mckesson.comabout-mckessoneeo-at-mckesson) page.
• Join us at McKesson!