Case processing skilled responsible for end-to-end ICSR processing within a large-volume OTC/consumer healthcare pharmacovigilance program, predominantly non-reliable 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 responsible 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
Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
📌 Pv Scientist Case Processing Mumbai
🏢 Soterius Life Sciences
📍 Mumbai
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.