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.
The Role
MLR review is one of the Life Science industry's biggest bottlenecks - and we're rebuilding it with AI.
Falcon MLR is Veeva's AI application for medical, legal, and regulatory (MLR) review. Our AI agents review promotional material the way expert reviewers do: against the actual rules of each market and the science behind the claims. We're looking for an MLR expert to take ownership of review quality across Europe.
You have sat in the review meetings. You know the codes, the process, and their pain points. Now, help build the reviewer and shape the future of MLR for the entire Life Science industry. You'll work directly with Falcon MLR's founding team, and your judgment will ship into a product used globally by the top Pharmaceutical companies.
We work like a start-up inside Veeva. The team is small, you own your area end to end, and your decisions reach the product fast. It suits people who like to build and take ownership.
Jobs that combine deep MLR expertise with frontier AI barely exist. This is one.
What You'll Do
Maximize reviewer agreement with Falcon's findings across our EU markets
Lead our regulatory monitoring system with engineering and product, and coordinate with other regions
Operationalize the reviewer-feedback loop, turning customer inputs into product improvements
Investigate, diagnose and resolve “why did Falcon flag this?” - read the agent's traces, find the root cause, fix it. Build the process for handling these questions with users
Automate recurring tasks with AI workflows
Ownership of quality benchmarks e.g. review quality, in cross functional collaboration with engineering and product
Requirements
You have been part of MLR/PRC review of promotional material - in pharma, biotech or at an agency serving one
You know the European codes - EFPIA, or national ones like ABPI, ENLI, FSA, Farmindustria, LEEM
You learn dense regulatory and legal material fast - and have results to show
AI is already part of your daily work – you have automated parts of your own job and want to go further
You have worked hands-on in Vault PromoMats - reviews, annotations, claims libraries
You live in the EU
#RemoteUK
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.
As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.
If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@veeva.com. 