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猎鹰MLR战略 - 美国

雇主

Veeva Systems

地点

远程 · Remote · 美国

待遇

$USD 120,000 - USD 180,000 / annual

工作模式

远程

截止日期

1月6日

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岗位摘要

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.

岗位职责

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.Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.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
You have been part of MLR/PRC review of promotional material - in pharma, biotech or at an agency serving one
You know the US rules - FDA/OPDP requirements and the PhRMA Code
You have reviewed both HCP- and consumer-directed promotional materials and can assess claims against the Prescribing Information and supporting evidence
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 high agency and entrepreneurial spirit - you have built something of your own, at work or outside it, and you do not wait to be told what to do
You have worked hands-on in Vault PromoMats - reviews, annotations, claims libraries
You live in the US
Nice to Have
You're on the US East Coast - your working day overlaps with our Copenhagen team
Interviewing with Veeva
We value your time and believe in a transparent hiring process. Here is the process you can expect.
Follow the application process and submit your resume.
If moving to the interview stage, our process is as follows:
A conversation with the hiring manager
A personality assessment
A practical case exercise
A final conversation with our group's Senior Leader
Once all interviews are complete, the manager will be in touch with a final decision.
Perks & Benefits
Medical, dental, vision, and basic life insurance
Flexible PTO and company paid holidays
Retirement programs
1% charitable giving program
Compensation
Base pay: $120,000 - $180,000
The salary range listed here has been provided to comply with local regulations and represents a potential base salary range for this role. Please note that actual salaries may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position may also be eligible for other types of compensation in addition to base salary, such as variable bonus and/or stock bonus.
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 .Originally posted on Himalayas

申请条件

- 具备MLR(医学、法律、法规)审查领域的深厚专业知识
- 熟悉美国市场的审查规则、行业准则和流程
- 拥有参与MLR审查会议的实际经验
- 了解MLR审查中的痛点、流程和规范
- 能够独立负责并端到端地管理美国市场的审查质量
- 具备与初创团队合作的能力,适应快节奏工作环境
- 能够将专业判断转化为产品决策并快速落地
- 有与AI产品团队协作的经验或意愿
- 具备跨职能协作能力,能与创始团队紧密合作
- 对生命科学行业和AI应用有热情
- 能够最大化审查员对AI审查结果的认可度
- 具备领导审查质量相关工作的能力

雇主简介

Veeva Systems 为生命科学行业提供行业云解决方案,包括应用、代理、数据和咨询服务,帮助生物制药公司加速药物开发。

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数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有