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Key Responsibilities:
- Take ownership of MLR review quality across the US market, maximizing reviewer agreement with Falcon's findings.
- Lead the regulatory monitoring system with engineering and product, coordinating with other regions.
- Operationalize the reviewer-feedback loop, turning customer inputs into product improvements.
Requirements:
- Have been part of MLR/PRC review of promotional material in pharma, biotech, or an agency.
- Know US FDA/OPDP requirements and the PhRMA Code.
- Have reviewed HCP- and consumer-directed promotional materials against Prescribing Information.
Our Values:
- We value flexibility with a Work Anywhere culture, supporting work from home or office.
- We are a public benefit corporation, legally bound to balance customer, employee, society, and investor interests.
- Our team operates like a start-up inside Veeva, with small teams and fast decision-making.
Veeva Systems
Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As a public benefit corporation and one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue with extensive growth potential ahead.