A global pharmaceutical solutions company in Oakville is looking for a Pharmacovigilance Associate to process Adverse Event data and ensure compliance with industry guidelines. The ideal candidate holds a Bachelor's degree in life sciences and has 1-2 years of relevant experience. Responsibilities include data entry, reporting, and acting as a liaison with internal and external stakeholders. This full-time position comes with a comprehensive benefits package and a salary range of CAD 48,500 - 74,690.
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Pharmacovigilance Analyst: AE & ADR Reporting • Oakville, ON, CA