Trainee Specialist Pharmacovigilance

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

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Qualification

• B.Pharm / M.Pharm

• BDS

• Life Science Graduate

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Experience

• Freshers / Entry-level candidates preferred

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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

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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

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