Pharmacovigilance Coordinator

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.