Assistant General Counsel

Role SummaryThis position with the Regeneron Regulatory and Commercial Law team will provide proactive and collaborative legal advice and counsel in connection with the commercialization of one or more of Regeneron’s products, and be part of a legal team supporting cardiovascular, hematology, rare disease, oncology, obesity, and new products. Counsel will be embedded as a core team member, serving as a strategic legal advisor to multiple internal stakeholders, including the commercial, medical affairs, regulatory, HEOR, corporate affairs, and compliance teams. Counsel will advise our internal partners through a deep understanding of (i) the complex laws and regulations and (ii) business and strategic objectives related to the discovery, development, and commercialization of biotechnology products. The ideal candidate will have relevant in‑house experience counseling on an approved product and providing practical and strategic legal advice on a broad range of issues.ResponsibilitiesProviding day‑to‑day strategic and business‑focused legal and risk counseling for one or more of Regeneron’s products/product candidates, from development through commercialization, including advising on a broad range of healthcare regulatory matters, including regulatory labeling discussions, advertising and promotion, drug safety, market research, scientific exchange and interactions with healthcare professionals and patients.Demonstrating a solid understanding of the strategic and tactical objectives of the client teams supported, and advising on strategic brand and medical planning, developing creative and innovative solutions to key initiatives, considering the business objectives and priorities, as well as the US and/or international legal and regulatory landscape.Counseling on all aspects of product commercialization, including launch preparation, launch execution, market development, disease awareness, product communication, advertising and promotion, and strategic brand planning.Ensuring compliance with all relevant laws, regulations, policies, procedures and controls within relevant business areas supported.Advising on data disclosures following clinical development milestones via press releases and US or international medical congresses and scientific exchange compliant with applicable laws and regulations.Liaising with other Law Department functions both in the US and globally, including litigation, IP, Compliance, and Transactions, to ensure integrated legal support and timely updates and information sharing.Reviewing relevant draft scientific publications and providing guidance as appropriate.Providing additional legal support on various matters for the Regulatory and Commercialization Law Team.QualificationsPrevious experience as a product attorney at a pharmaceutical or biotechnology company preferred.Ability to handle multiple priorities in a dynamic and evolving environment.Excellent oral and written communication skills with a shown ability to present complex information accurately and concisely to influence others at all levels of management.Proven capacity to cultivate strong client relationships and influence leadership, including ability to assess and help business colleagues handle risks in a highly regulated environment.Strong analytical skills and demonstrated learning agility and a deep aptitude for science and data analysis.Committed to teamwork and collaboration across multiple functional areas.EducationJD with excellent law school credentials. Licensed to practice law in New York or eligible for licensure as in‑house counsel. 10+ years of legal experience, including positions as an in‑house attorney at a biotech/pharmaceutical company, and at a nationally recognized law practice in pharmaceutical and healthcare law. Solid understanding of the biotech/pharmaceutical industry, including product development, commercialization, and the legal and regulatory environment (including healthcare fraud and abuse, anti‑kickback, and competition law). Deep knowledge of applicable statutory and regulatory frameworks governing the sale and marketing of biopharmaceuticals.Additional RequirementsThis role is based at Regeneron’s offices in Sleepy Hollow, NY (4 days a week onsite) – it is not open to hybrid or fully remote assignments. #J-18808-Ljbffr