• Initiate communication with internal business teams and subsidiaries for SDEA requirements
• Follow up with third-party partners to establish and maintain SDEAs
• Perform timely exchange of safety data with business partners
• Conduct adverse event reconciliation with partners
• Support case processing and safety writing activities
• Ensure compliance with global pharmacovigilance standards
• Stay updated with current PV regulations and scientific developments
• B.Pharm / M.Pharm / BAMS / BHMS
• 3–4 years of experience in pharmacovigilance
• Hands-on experience in case processing, safety writing and SDEA management
• Experience in safety data exchange and reconciliation activities
• Knowledge of global pharmacovigilance regulations
• SDEA management & reconciliation
• Case processing & safety writing
• Strong written and verbal communication skills
• Presentation & documentation skills
• A leading life sciences organization engaged in delivering high-quality pharmacovigilance and drug safety solutions across global markets
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