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 the US.
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 the US market
- 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
Nice to Have
Interviewing with Veeva
We value your time and believe in a transparent hiring process. Here is the process you can expect.- A conversation with the hiring manager
- A personality assessment (unless you have already completed it with Veeva previously)
- A practical case exercise
- A final conversation with our group's Senior Leader
Perks & Benefits
Compensation
#LI-RemoteUS
#LI-MidSenior
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world. Veeva is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin or ancestry, age, disability, marital status, pregnancy, protected veteran status, protected genetic information, political affiliation, or any other characteristics protected by local laws, regulations, or ordinances. 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 [email protected].
Skills
Medical Legal Regulatory (MLR) Review — Pharmaceutical Compliance — AI/Machine Learning — Regulatory Code Knowledge — Quality Assurance — Product Strategy — Life Sciences Domain Expertise — Process Optimization