Turn detailed safety information into accurate pharmacovigilance records at Cencora. Use strong communication, organization, and problem-solving skills across assigned activities.
As a Drug Safety Associate, you will process adverse event information and product quality complaints for client programs. Cencora seeks candidates with one to three years of experience in Medical Information, Clinical Research, Drug Safety, pharmacy, or pharmaceutical fields. The work includes clarifying information with internal and external clients, conducting quality checks, and supporting source data verification. Current knowledge of Health Canada, US FDA, EMEA, and ICH guidelines is important.
Key Responsibilities: Request clarification and additional information from clients




Perform quality checks on adverse event reports
Assist with source data verification checks
Prepare transcription, translation, and redaction activities
Support non-conformance and CAPA processes
Requirements: College-level education is required
Life Sciences concentration is a robust asset
Effective oral and written communication skills
Superior attention to detail and deadline consistency
Effective interpersonal and multitasking abilities
Bring careful review, client communication, and pharmacovigilance expertise to Cencora’s adverse event and complaint workflows.

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📌 Pharmacovigilance Drug Safety Specialist (Manitoba)
🏢 Innomar Strategies
📍 Manitoba