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Role & Responsibilities
Perform triage and initial validity assessment of adverse event cases
Enter and manage safety data in global pharmacovigilance databases
Conduct initial ICSR assessments as per regulatory requirements
Evaluate cases for expedited reporting and regulatory timelines
Prepare and submit CIOMS I, MedWatch and XML safety reports
Draft follow-up queries to collect missing case information
Maintain audit-ready documentation
Retrieve and assess cases from EVWEB and health authority sources
Support additional pharmacovigilance activities as assigned
Qualification
B.Pharm / M.Pharm
BDS
Life Science Graduate
Experience
Freshers / Entry-level candidates preferred
Skills
Strong written and verbal communication
Attention to detail and compliance mindset
Basic understanding of pharmacovigilance and drug safety
Willingness to learn global PV regulations
Time management and documentation skills
About the Company
Cencora, through PharmaLex India, is a global healthcare services organisation delivering regulatory, pharmacovigilance and risk management solutions while ensuring patient safety and compliance across international markets