Pharmacovigilance Coordinator (6-month contract) Remote - Ontario OR Quebec
Responsibilities
- 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.
- Cross-Functional Collaboration: Work closely with cross-functional teams, including regulatory, quality assurance, and medical affairs, to align on safety processes and requirements.
Requirements
- Bachelor's Degree in Science, or related field
- Experience: 3+ years of experience in pharmacovigilance, patient/drug safety.
- Language: French/English bilingual preferred.
- 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.