• Provide thought leadership expertise via analyses and external dissemination of key regulatory insights and implications on commercialization strategies • Understand intersection of regulatory strategy with commercial and market access stakeholders • Drive business development with key regulatory affairs and intelligence professionals within the biopharmaceutical and biotech industry  • Ability to speak and write thoughtfully on such matters to a variety of audiences, internally and externally • Interface with a portfolio of Avalere Health clients, managing and anticipating specific client needs • Lead and contribute to broader projects (e.g., policy, market access, evidence, global) as a regulatory subject matter expert • Solve complex client queries related to governing statute, applicable regulations and technical guidance on drug development and FDA oversight with rigor and agility • Build industry partnerships and connections to deepen Avalere’s strategic visibility in regulatory strategy and FDA policy • Lead, manage, supervise, train and mentor junior and mid-level staff members across the firm • Possess critical thinking, curiosity and an eagerness to connect the dots from historic precedents to upcoming business implications • Represent Avalere Health in public forums (e.g., webinars, conference panels, etc.)