Become a crucial part of healthcare safety as a Pharmacovigilance Specialist focused on medical information management. This role demands your expertise in evaluating and reporting adverse events promptly.
In this key role, you will drive pharmacovigilance efforts by screening reports and liaising with partners. You will conduct medical reviews, assess scientific validity of documents, and ensure compliance with Health Canada and ICH requirements. This position is essential for those looking to contribute significantly to product safety initiatives.
Key Responsibilities:
• Perform ICSR report triage and assessments
• Submit timely adverse event reports to Health Canada
• Liaise with partners for product safety improvements
• Conduct comprehensive medical reviews and literature analyses
• Prepare for inspections and audits as required
Requirements:
• Science Degree with three years of pharmacovigilance experience
• Comprehensive knowledge of Canadian GMPs a...