Trainee Specialist Pharmacovigilance
About the Role
About the role & responsibilities
• Perform triage and validity assessment of adverse event reports
• Enter and process ICSRs in global safety databases
• Assess cases for expedited reporting timelines
• Prepare CIOMS, MedWatch and XML safety reports
• Draft follow-up queries to obtain missing case information
• Retrieve and review EVWEB cases
• Maintain audit-ready safety documentation
• Support additional pharmacovigilance activities
Qualification
• B.Pharm / M.Pharm
• BDS
• Life Science graduate
Experience
• Freshers and early-career candidates eligible
Skills
• Pharmacovigilance and ICSR processing knowledge
• Strong communication skills
• High attention to detail
• Ability to meet regulatory timelines
About the company
• Cencora (PharmaLex India Private Limited) is a global healthcare services organization focused on drug safety and regulatory compliance
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