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.
Communication: Serve as a liaison with internal and external stakeholders to address safety-related inquiries and provide updates.
Compliance: Ensure adherence to all relevant regulations, guidelines, and standard operating procedures.

Essential skills and knowledge

Requirements

Communication Skills: Strong verbal and written communication skills, with the ability to collaborate effectively across teams.
Attention to Detail: Exceptional ability to review and process detailed medical and regulatory forms accurately.
Independence: Self-starter with the ability to work independently and manage competing priorities.
Tech Savvy: Comfortable using pharmacovigilance systems, data management tools, and standard office software.
Adaptability: Ability to hit the ground running and adapt to evolving workflows and timelines.
Experience: Prior experience in pharmacovigilance, regulatory affairs, or related medical fields is an asset.

Related tags

JOB SUMMARY

Pharmacovigilance Specialist

Toronto

5 days ago

Entry / Junior

Full-time