Santhiya Srinivasan

At Accenture, I support global safety processes, local pharmacovigilance compliance, and quality oversight as a Senior Drug Safety Scientist. I provide subject matter guidance to cross-functional teams, lead training for affiliate staff, and contribute to client meetings, SLA/KPI compliance, and process improvement.

I've managed end-to-end safety case processing, from intake and triage through coding, narrative writing, follow-up, quality review, and safety communications. My work includes duplicate checks, reconciliation, literature monitoring, regulatory documentation, and country-specific adverse event reporting.

I work across Oracle Argus, ArisG, MedDRA, WHO-DD coding, safety databases, and regulatory reporting activities. I've also supported automation and UAT testing initiatives, AI-driven safety improvements, audits, late-case investigations, and global activities across EU, US, Asia, the Middle East, and Africa.

With 7+ years in drug safety, I bring a practical focus on compliance, accurate delivery, operational excellence, and mentoring new team members.