Pharmacovigilance Specialist

Job Summary

Working remotely in a full-time capacity, the Pharmacovigilance Specialist will manage adverse event submission compliance, ensure adherence to operational processes within the Argus database, and support periodic reporting and submission projects.

Key responsibilities

• Monitor and execute expedited and non-expedited individual case safety report (ICSR) submissions and exchanges
• Generate and verify custom reports for Periodic Safety Reports while assisting in the setup of health authority requirements
• Conduct performance qualification testing for Argus upgrades and execute updates for new territory-specific E2B profiles

Required qualifications

• Post-secondary education or equivalent professional experience; a life science degree is preferred
• At least 2 years of proven experience in a similar role
• C1 level proficiency in English
• Proficient in Microsoft Office Suite and computer keyboarding skills
• Ability to work independently and collaboratively within a multidisciplinary team