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Role & Responsibilities
Perform end-to-end ICSR case processing
Triage, prioritize and assess adverse event cases
Conduct MedDRA and WHO-Drug coding
Assess seriousness, causality and expectedness
Draft narratives and sender comments
Manage follow-ups, reconciliations and regulatory timelines
Support inspections, audits and safety surveillance activities
Handle literature review and mailbox management
Qualification
Bachelor of Ayurvedic Medicine and Surgery (BAMS)
Bachelor’s Degree in Life Sciences
Master’s Degree in Life Sciences
Experience
1–3 years of pharmacovigilance experience
Skills
Strong knowledge of pharmacovigilance workflows
Good command over MedDRA and WHO-Drug coding
Medical writing and documentation skills
Proficiency in MS Office tools
Excellent communication and compliance orientation
About the Company
Accenture is a global professional services organization with large-scale life sciences operations
Works with international clients and regulatory frameworks
Offers long-term growth in drug safety and pharmacovigilance careers