Pharmacovigilance Specialist, Submissions

ProPharma seeks a Pharmacovigilance Specialist, Submissions to ensure adverse event submission compliance with health authorities, ethics committees, institutional review boards, and safety partners. The Specialist will work within the multi-tenant Argus database to track adverse event reports and maintain compliance with regulations.

Requirements

• Post-secondary education or equivalent professional work experience
• Fluent in English
• Proven experience in a similar role
• Proficient computer knowledge, specifically Microsoft Office Suite
• Excellent attention to detail
• Strong verbal, written and interpersonal communication skills
• Flexibility to adapt and meet fluctuating business priorities
• Ability to work independently and collaboratively in a multidisciplinary team