Join Cencora as a Remote Drug Safety Associate, contributing to patient support and pharma commercialization services. Leverage your clinical data skills while making a difference in health outcomes.

This full time role supports Cencora’s impactful services through Innomar Strategies. Ideal candidates will engage with clinical information, ensuring compliance with SOPs and applicable legislation. You will analyze source data documents and manage adverse event reporting, enhanced by your knowledge of the pharmacovigilance industry.

Key Responsibilities:
• Receive and document clinical information in compliance with SOPs
• Collaborate with clients for information verification and clarification
• Review source data, triaging adverse events and product complaints




• Ensure quality checks on adverse event reports as needed
• Assist in source data verification and reconciliation report preparation

Requirements:
• Minimum college-level education, preferably in Life Sciences
• 1-3 years in Medical Information or Clinical Research
• Knowledge of pharmacovigilance guidelines
• Strong analytical and organizational skills
• Bilingual in English/French is an asset

Utilize your attention to detail and problem-solving skills as part of Cencora’s committed team.
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📌 Remote Drug Safety Associate at Cencora (New Brunswick)
🏢 Innomar Strategies
📍 New Brunswick