Pharmacovigilance Services New Associate

Role & Responsibilities

• Perform end-to-end ICSR processing for AE, SAE and SUSAR cases

• Identify, triage and create cases in global safety databases

• Review source documents for validity and medical relevance

• Perform MedDRA and WHO-Drug coding

• Draft case narratives and E2B sender comments

• Manage follow-ups, reconciliations and regulatory timelines

• Support audits, inspections and pharmacovigilance projects

• Handle literature intake, mailbox monitoring and translations

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Qualification

• B.Pharm

• BSc Nursing

• Bachelor’s Degree in Life Sciences

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Experience

• 0–1 year (Freshers eligible)

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Skills

• Basic knowledge of pharmacovigilance and ICSR workflows

• Familiarity with MedDRA and WHO-Drug

• Good documentation and MS Office skills

• Strong English communication skills

• Ability to work in compliance-driven environments

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• About the Company

  • Accenture is a global professional services leader operating in over 120 countries

  • Delivers technology-driven healthcare and life sciences solutions

  • Provides structured career growth and global exposure in pharmacovigilance