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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
Qualification
B.Pharm
BSc Nursing
Bachelor’s Degree in Life Sciences
Experience
0–1 year (Freshers eligible)
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
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