Join Cencora's mission to enhance patient safety as a Drug Safety Associate. This full-time role focuses on pharmacovigilance, data entry, and compliance within a team-oriented environment.

As a vital part of Cencora’s Innomar Strategies team, you will support patient and provider safety initiatives. Your responsibilities include reviewing clinical data, documenting adverse events, and ensuring compliance with industry regulations. This is an excellent opportunity for someone with a background in life sciences to contribute to meaningful health solutions.

Key Responsibilities:
• Receive and document clinical information according to protocols
• Review source data and triage adverse event information




• Enter adverse event data into specific databases
• Perform quality checks on reports and source data verification
• Screen literature for relevant safety information

Requirements:
• Minimum college level education required
• 1-3 years experience in Medical Information or Drug Safety
• Up-to-date knowledge of pharmacovigilance regulations
• Strong analytical and organizational skills
• Bilingual in English/French is an asset

Make a difference by ensuring the safety of patients and products at Cencora.
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📌 Drug Safety Associate at Cencora (Quebec City)
🏢 Innomar Strategies
📍 Quebec City