Associate

• Lead the collection, evaluation, and processing of adverse event reports in accordance with regulatory guidelines and company policies
• Conduct data analysis and interpretation of safety data, identifying trends and potential safety signals
• Prepare and submit periodic safety update reports (PSURs) and other regulatory documents
• Collaborate with medical and clinical teams to assess the clinical relevance of adverse events and contribute to risk management activities
• Oversee the maintenance and integrity of pharmacovigilance databases
• Provide training and mentorship to junior team members
• Engage in regulatory audits and inspections, ensuring readiness and compliance

Associate jobs in Chile

Senior Pharmacovigilance Associate