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.