EU MLR Strategy Lead — AI-Driven Regulatory Review

Veeva Systems, Inc.; Greater London; Hybrid; GBP 90,000 - 120,000; Full time

Benefits offered by this job

Paid Maternity & Paternity Leave

Global Mobile phone & Internet Policy

Veeva 1% Giving

Fitness Reimbursements

Veeva Break

Job summary

Veeva Systems, a mission-driven leader in life sciences software, seeks an MLR expert to own review quality across Europe. You will work with Falcon MLR's founding team to align promotional material with market rules and science, leveraging AI to improve reviewer accuracy.

Team size is small; you own your area end to end, shaping a product used by top pharma clients worldwide. The role requires deep MLR expertise, fluency with European codes, and a drive to advance AI-enabled regulatory

Qualifications

• You have been part of MLR/PRC review of promotional material in pharma, biotech or agency service.
• Knowledge of European codes (EFPIA, ABPI, ENLI, FSA, Farmindustria, LEEM).
• Ability to learn dense regulatory material quickly and show results.
• Experience with AI integration into daily work and automation.

Responsibilities

• Maximize reviewer agreement with Falcon's findings across EU markets.
• Lead regulatory monitoring with engineering and product, coordinating with regions.
• Operationalize reviewer-feedback loops and translate inputs into product improvements.
• Investigate 'why did Falcon flag this?' by tracing agent results and fixing root causes.
• Automate recurring tasks with AI workflows.
• Own quality benchmarks in collaboration with engineering and product.

Skills

MLR review

Regulatory knowledge

AI workflows

Tools

Vault PromoMats

Job description

Veeva Systems, a mission-driven leader in life sciences software, seeks an MLR expert to own review quality across Europe. You will work with Falcon MLR's founding team to align promotional material with market rules and science, leveraging AI to improve reviewer accuracy.

Team size is small; you own your area end to end, shaping a product used by top pharma clients worldwide. The role requires deep MLR expertise, fluency with European codes, and a drive to advance AI-enabled regulatory