PV Scientist - Case Processing

Role Overview:

Case processing professional responsible for end-to-end ICSR processing within a large-volume OTC/consumer healthcare pharmacovigilance program, predominantly non-serious cases. An entry-level scientific role covering the full case lifecycle, with structured training provided

Qualification and Experience:

• Degree in Pharmacy, Pharm D, BHMS, BDS or equivalent preferred
• At least 6 months of related experience in pharmacovigilance, drug safety, or allied clinical, scientific, or safety domains (trainable)

Key Responsibilities:

• Perform case intake, book-in, triage, and validity assessment in line with program SOPs.
• Carry out ICSR data entry, MedDRA coding, and narrative writing as per defined timelines.
• Manage E2B submissions and case follow-up activities.
• Maintain quality and compliance across all activities.
• Escalate complex or potentially serious cases appropriately.
• Participate in training and development to build case processing competency.

Key Skills:

• End-to-end case processing - intake, triage, submission, data entry, follow-up
• MedDRA coding
• Narrative writing
• Safety database knowledge - Argus, LSMV, Veeva or equivalent
• Quality and compliance
• Consumer health

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