Advance drug safety operations with Sentrex Health Solutions through adverse event triage, case reporting, and detailed pharmacovigilance documentation in Markham.
As a full-time Pharmacovigilance Associate, you will manage safety information across manufacturers and patient assistance programs. The role requires familiarity with Health Canada GVP regulations, GxP processes, reporting timelines, and quality standards. You will also help maintain audit readiness and support stakeholders with case queries.
Key Responsibilities: Manage pharmacovigilance inboxes and organize incoming safety information
Recognize, triage, record, and report adverse event data
Track stakeholder and manufacturer queries within reporting timelines
Prepare documentation and files for pharmacovigilance audits




Conduct periodic case reconciliation with departments and clients
Requirements: Three-plus years of pharmacovigilance or relevant industry experience
Three-plus years working in pharmaceutical environments
Knowledge of Health Canada GVP and GxP requirements
Exceptional attention to detail and organizational ability
Team-oriented communication and effective problem-solving skills
Bring drug safety knowledge, accurate case handling, and regulatory awareness to Sentrex Health Solutions’ pharmacovigilance team.

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📌 Drug Safety Associate Health Canada (Ontario)
🏢 Sentrex Health Solutions
📍 Ontario