About role & responsibilities
• Perform triage and initial validity assessment of adverse event cases
• Process spontaneous, clinical trial, literature and authority safety reports
• Enter safety data accurately into pharmacovigilance databases
• Conduct initial ICSR assessments as per global regulatory requirements
• Evaluate cases for expedited reporting timelines
• Prepare and submit CIOMS I, MedWatch and XML safety reports
• Draft and manage follow-up queries to collect missing information
• Maintain audit-ready case documentation
• Retrieve and review EVWEB company and non-company cases
• Support additional pharmacovigilance activities as assigned
Qualification
• B.Pharm
• M.Pharm
• BDS
• Life Science Graduate
Skills
• Strong written and verbal communication
• High attention to detail
• Basic understanding of pharmacovigilance and drug safety reporting
• Ability to work within strict regulatory timelines
• Willingness to learn global PV regulations
Experience
• Freshers and early-career professionals can apply
Salary
• ₹3,00,000 – ₹5,00,000 per annum (estimated)
Benefits
• Comprehensive training in global pharmacovigilance operations
• Exposure to international regulatory standards and safety systems
• Career growth within Cencora / PharmaLex
• Inclusive and equal-opportunity work culture
About the company
• Cencora (PharmaLex India Private Limited) is a global healthcare services organization
• Focused on pharmacovigilance, regulatory compliance and risk management
• Committed to patient safety, diversity and inclusive workplace practices