Job Title

Introduction We are hiring a Pharmacovigilance Coordinator for our client, a reputable and leading pharmaceuticals company globally, based in Toronto, Ontario. This is a 6-month contract working full-time hybrid, with the possibility of extension. The Pharmacovigilance Coordinator will conduct thorough reviews of medical forms, ensuring accuracy and compliance with pharmacovigilance standards to contribute to the companys commitment to patient safety. Cross-Functional Collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements. Adverse Event Management: Monitor, document, and report adverse events in compliance with regulatory guidelines. Data Management: Enter and maintain accurate data in pharmacovigilance systems, ensuring timely updates and reports. Attention to Detail: Exceptional ability to review and process detailed medical and regulatory forms accurately. Tech Savvy: Comfortable using pharmacovigilance systems, data management tools, and standard office software. Prior experience in pharmacovigilance, regulatory affairs, or related medical fields is an asset. Finding the next step in your career can be a fulltime job in itself. Over 45 years, weve created a global network of interesting clients and talented individuals working together through a vast array of services.