Senior Safety Domain Expert

What you'll do

• Advise product and engineering teams on safety case intake, triage, validation, and data reconciliation workflows.
• Verify platform outputs for initial data entry, automated MedDRA coding, and generated follow-up queries.
• Translate feedback from early adopter organizations into actionable improvements for the platform.
• Map out complex, multi-variable safety case scenarios to test and calibrate the platform's reasoning boundaries.
• Act as the "Voice of the Customer" to ensure the delivery of high-quality safety automation tools.
• Provide expert guidance on global compliance, MedDRA coding rules, and safety database requirements.

What we're looking for

• Must have 5+ years of active experience in Pharmacovigilance or Drug Safety Operations.
• Must possess extensive hands-on knowledge of the complete case lifecycle, including validation criteria and global reporting timelines.
• Must have high proficiency with MedDRA coding rules.
• Must be familiar with mainstream safety databases such as Veeva Safety, Argus, or ArisG.
• Must possess a strong collaborative mindset to present operational perspectives to technical partners and customers.
• Prior experience contributing to the design, implementation, or UAT of automated pharmacovigilance intake solutions (preferred).
• Prior experience with or interest in agentic AI, automated workflows, or next-generation cloud platforms (preferred).