---
title: "Valli Vinayagam - safety science analyst in Greater Chennai Area | Tal"
description: "Meet Valli Vinayagam, Safety Science Analyst | End-to-End ICSR Processing & SAE Reporting | Pharmacovigilance @ Fortrea based in Greater Chennai Area."
image: "https://tal.club/meet/valli-1/share-image"
---

# Valli Vinayagam on Tal

## Headline

Safety Science Analyst \| End\-to\-End ICSR Processing &amp; SAE Reporting \| Pharmacovigilance @ Fortrea

## About

Every drug on the market has a safety story behind it\. I'm one of the people who documents it\. As a Safety Science Analyst at Fortrea, I manage the end\-to\-end lifecycle of Individual Case Safety Reports \(ICSRs\) — from intake and data entry through narrative writing, quality review\. I handle spontaneous case processing, SAE and adverse event reporting, follow\-up management, and case nullification, working within strict global pharmacovigilance timelines and ICH E2B standards\. In my first year, I've built a working knowledge of the full PV workflow: triaging incoming safety data, applying medical judgment to case narratives, and maintaining data integrity through quality review cycles\. I understand what it takes to keep a safety database clean and a regulatory dossier defensible\. My background in pharmacy gives me the clinical foundation to assess cases accurately — not just process them\. That difference matters when a regulator asks questions\. 📌 If you're hiring for pharmacovigilance roles — ICSR processing, safety reporting, or drug safety operations — let's talk\. Open to opportunities across India and globally\.

## Location

Greater Chennai Area

## Work experience

safety science analyst at Fortrea, Jul 2025 \- Jun 2026 · 1 yr, Bengaluru, Karnataka, India, Safety Science Analyst · Fortrea • Ensured zero late submissions on ICSR cases by managing end\-to\-end case processing — from intake through narrative writing and quality review — within regulatory reporting windows\. • Maintained data accuracy across a high\-volume spontaneous case processing workflow by applying ICH E2B standards and conducting systematic quality checks, reducing rework on case records\. • Strengthened regulatory defensibility of safety narratives by applying clinical pharmacy knowledge to accurately characterise adverse events, resulting in cleaner, audit\-ready case documentation\. • Managed follow\-up outreach and case nullification/deletion requests across multiple safety databases, ensuring case lifecycle completeness and database integrity for regulatory submissions\. • Supported cross\-functional safety data review by coordinating workflow management tasks and flagging signal\-relevant cases for pharmacovigilance scientists, contributing to team efficiency in case triage\.

Pharmaceutical Production Technician at Sai Mirra Innopharm, Sep 2024 \- Oct 2024 · 2 mos, Ambattur, Tamil Nadu, India

Pharmacist at Sri kumaran pharmacy, Aug 2024 \- Oct 2024 · 3 mos, Āvadi, Tamil Nadu, India

## Education

Bachelor of Pharmacy \- BPharm, Pharmacy, Jaya College Of Pharmacy

Mathematical Biology, Kanchi sri sankara academy matric Hr\. Sec\. School

[View the original profile](https://tal.club/meet/valli-1)

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