PV Scientist - Case Processing

Soterius Life Sciences; Mumbai; On-site; INR 300,000 - 420,000; Full time

Job summary

Soterius Life Sciences is seeking an entry-level Case Processing Professional to support end-to-end ICSR processing in a high-volume pharmacovigilance program. The role covers intake, triage, data entry, coding, and narrative writing with structured training provided.

You will work on MedDRA coding, E2B submissions, and ensure quality and compliance across the case lifecycle, with emphasis on learning and accuracy in a consumer health setting.

Qualifications

• Degree in Pharmacy, PharmD, BHMS, BDS or equivalent preferred.
• At least 6 months of related experience in pharmacovigilance, drug safety, or allied clinical, scientific, or safety domains (trainable).
• Entry-level role covering full case lifecycle with structured training provided.

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.

Skills

End-to-end case processing

MedDRA coding

Narrative writing

Safety database knowledge

Quality and compliance

Consumer health

Education

Pharmacy/PharmD/BHMS/BDS or equivalent

Tools

Argus

LSMV

Veeva

Job description

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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