Senior Safety Domain Expert - Falcon

About this role

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last fiscal year with extensive growth potential ahead.

At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.

Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.

The Role
We are looking for an experienced pharmacovigilance professional to serve as our Senior Safety Domain Expert for Veeva Falcon. This role bridges ground-level case execution with macro-level safety operations, using your deep knowledge of case processing, MedDRA coding, database reconciliation, and global compliance to inform our AI driven automation tools. You will spend your days collaborating with our internal technical teams and external early adopters, acting as the definitive "Voice of the Customer" to ensure our platform delivers flawless safety automation.

End-to-End Workflow Guidance: Advise product and engineering teams on the detailed steps of safety case intake, triage, validation, and advanced data reconciliation workflows

Ground-Truth Verification: Actively review and verify platform outputs across initial data entry, automated MedDRA coding assignment, and generated follow-up queries to ensure absolute data precision

Early Adopter Engagement: Interact directly with PV leads and processing specialists at early adopter organizations, translating their feedback into actionable platform enhancements

Stress-Test Scenario Building: Map out highly complex, multi-variable safety case scenarios to rigorously evaluate and calibrate the platform's reasoning boundaries 5+ years of active experience in Pharmacovigilance / Drug Safety Operations

Extensive hands-on knowledge of the complete case lifecycle, including validation criteria, database reconciliation, and global expedited reporting timelines

High proficiency with MedDRA coding rules and deep familiarity with mainstream safety databases (e.g., Veeva Safety, Argus, ArisG)

Strong collaborative mindset with the ability to confidently present operational perspectives to non-clinical technical partners and customers Prior experience contributing to the design, implementation, or user-acceptance testing (UAT) of automated pharmacovigilance intake solutions

Prior experience with, or a strong baseline curiosity about, agentic AI, automated workflows, or next-generation cloud platforms in clinical trials Medical, dental, vision, and basic life insurance

Flexible PTO and company paid holidays

Retirement programs

1% charitable giving program Base pay: $120,000 - $180,000

The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.