MLR Strategy

Veeva Systems

Confirmed live 2 days ago High trust
Remote

Quick summary

Work type
Remote
Location
Remote
Salary
$120,000–$180,000 / yr
Posted
31 days ago
Freshness
Confirmed live 2 days ago

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $201k
This role $150k
$106k most similar roles pay here $255k

This role pays less than 80% of similar roles. Most pay $161,437–$240,437 — the shaded band above. At the midpoint, this role pays about $150k versus about $201k for comparable roles.

Based on 240 similar postings.

Employer

About Veeva Systems

Veeva Systems is a cloud software company serving the global life sciences industry, providing CRM, clinical, regulatory, quality, and data applications used by pharmaceutical and biotech companies.

Veeva Systems currently has 93 open roles on FindRole.

Listed pay typically runs $80,000–$165,000 across 82 roles with salary data.

Most-posted roles

View all roles at Veeva Systems

At a glance

TL;DR · MLR Strategy

The Falcon MLR Strategy - US role is situated within the Strategy team. This position focuses on rebuilding medical, legal, and regulatory review processes by integrating AI to automate the evaluation of promotional materials against specific market rules and scientific claims. The successful candidate will take ownership of review quality across the US market, lead regulatory monitoring systems in collaboration with engineering and product teams, and operationalize feedback loops to drive product improvements. Key responsibilities include investigating agent traces to resolve technical issues, automating recurring tasks via AI workflows, and establishing quality benchmarks. Required expertise includes deep knowledge of FDA/OPDP requirements, the PhRMA Code, and experience with Vault PromoMats. The role requires a candidate who can navigate complex regulatory content while utilizing AI tools to solve bottlenecks in the life sciences industry.

What you'll do

  • Maximize reviewer agreement with Falcon's AI findings across the US market.
  • Lead the regulatory monitoring system in collaboration with engineering and product teams.
  • Operationalize the reviewer-feedback loop to turn customer inputs into product improvements.
  • Investigate, diagnose, and resolve root causes for specific AI flags by reviewing agent traces.
  • Build processes for handling technical and logic questions from users regarding AI findings.
  • Automate recurring manual tasks using specialized AI workflows.
  • Own quality benchmarks for review accuracy in cross-functional collaboration with engineering and product teams.

What we're looking for

  • You must have experience in MLR/PRC review of promotional materials for pharma, biotech, or at a serving agency.
  • You must possess knowledge of US rules, including FDA/OPDP requirements and the PhRMA Code.
  • You must be able to assess claims against Prescribing Information and supporting evidence for both HCP and consumer materials.
  • You must have hands-on experience in Vault PromoMats, specifically with reviews, annotations, and claims libraries.
  • You must demonstrate the ability to learn dense regulatory and legal material quickly.
  • You should have experience using AI tools in your daily work to automate tasks.
  • You must possess an entrepreneurial spirit and high agency to take ownership of projects independently.
  • You must reside in the United States.

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