GoodRx is the leading prescription savings platform in the U.S. Trusted by more than 25 million consumers and 750,000 healthcare professionals annually, GoodRx provides access to savings and affordability options for generic and brand-name medications at more than 70,000 pharmacies nationwide, as well as comprehensive healthcare research and information. Since 2011, GoodRx has helped consumers save nearly $75 billion on the cost of their prescriptions.
Our goal is to help Americans find convenient and affordable healthcare. We offer solutions for consumers, employers, health plans, and anyone else who shares our desire to provide affordable prescriptions to all Americans.
About the Role:
GoodRx is seeking a Healthcare Regulatory Counsel to independently handle complex legal matters spanning employee benefits contracts, healthcare regulatory product reviews, and artificial intelligence initiatives. This role provides practical legal guidance that helps teams evaluate risk, structure agreements, and bring products and programs to market responsibly.
As a senior individual contributor, you will apply broad expertise across related legal disciplines, lead legal reviews from intake through resolution, and help prioritize competing projects. You will partner with business leaders and legal colleagues to resolve novel issues, develop scalable review processes, and escalate significant risks or matters requiring specialized expertise. This role has no direct reports.
Responsibilities :
Independently draft, review, and negotiate employee benefits vendor and service agreements, amendments, and renewals in partnership with Total Rewards, Procurement, Finance, and other stakeholders. Address service commitments, fees, data use, confidentiality, liability, indemnification, termination, and applicable compliance obligations.
Identify benefits-related regulatory and contractual issues, coordinate with privacy and security partners, and engage specialized benefits counsel on complex plan, tax, or fiduciary matters as appropriate.
Lead healthcare regulatory legal reviews of new and existing products, features, programs, and partnerships from concept through launch. Translate complex requirements into clear recommendations, practical alternatives, and appropriate safeguards.
Assess applicable federal and state healthcare requirements involving pharmacy, telehealth, professional licensure, corporate practice of medicine, healthcare fraud and abuse, referral arrangements, and consumer-facing healthcare activities; coordinate with subject matter experts as needed.
Review proposed AI tools, vendors, features, and use cases in partnership with Product, Engineering, Privacy, Information Security, and Compliance. Evaluate healthcare regulatory implications, intended use, data handling, transparency, human oversight, and relevant contractual protections.
Help develop and apply AI review criteria and approval processes; document recommendations and escalate novel, high-impact, or unresolved risks to the appropriate legal leaders and business decision makers.
Triage incoming contracts and regulatory projects by clarifying scope, identifying risks and dependencies, recommending priorities, and coordinating ownership across legal and business teams. Manage assigned matters through completion and communicate status and timing.
Exercise independent judgment on significant and ambiguous issues, explain tradeoffs to diverse stakeholders, and recommend actionable paths that support business objectives and appropriate risk management.
Monitor relevant legal and regulatory developments, assess their implications for GoodRx, and recommend updates to contracts, product requirements, internal guidance, and review practices.
Develop templates, contract playbooks, review checklists, and training that improve consistency and efficiency. Serve as a trusted subject matter resource and contribute to cross-functional initiatives and other legal matters as…