Full Time

Trainee Specialist Pharmacovigilance

Cencora
Noida
₹3 - ₹5 LPA
Posted 30/12/2025

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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