Family Access Manager (FAM), Skeletal Dysplasia - MIDWEST

Role: Family Access Manager (FAM) supporting BridgeBio's rare disease portfolio, specifically for the infigratinib product. Primary objectives include educating families and care partners on access, affordability, and reimbursement processes, supporting patient journey, and executing launch activities. Responsibilities encompass providing personalized access support, collaborating with cross-functional teams (Market Access, Commercial, Legal, Compliance, Advocacy), managing patient support programs (ForgingBridges), and facilitating in-person or remote education. The role involves developing and implementing tactical access plans, ensuring compliance with healthcare regulations, and reporting insights. Qualifications: BA/BS preferred; 5-8+ years in biotech/pharma, with experience in patient services, Market Access, or hub models; rare disease experience advantageous. Skills include strong communication, relationship-building, analytical thinking, and familiarity with reimbursement challenges and patient support programs. High-value specifics include focus on rare diseases, specialty market understanding, and patient-centered programs. Work setup is hybrid with 40-60% domestic travel, primarily in Chicago, Minneapolis, or St. Louis regions. The role demands independent and team-oriented work in a fast-paced environment.