Sr. Medical Director, Medical Affairs

Role Summary

The Sr. Medical Director, Medical Affairs is a senior medical and scientific leadership role within Medical Affairs. This role is responsible for supporting the development and execution of the medical strategy for encaleret across clinical development programs, including autosomal dominant hypocalcemia type 1 (ADH1) and chronic hypoparathyroidism. The position is critical to advancing scientific engagement, evidence generation and dissemination, clinical development support, and lifecycle planning, and to preparing for United States launch and post marketing activities. The role will serve as a key cross-functional partner, providing medical expertise and strategic leadership and partnership across Clinical Development, Regulatory, Commercial, Patient Advocacy, and Field Medical, and will represent BridgeBio externally with investigators, KOLs, patient organizations, and the broader scientific community. Location can be remote or hybrid/on-site (San Francisco Bay Area); ability to travel up to ~40% is expected for scientific meetings, advisory boards, and internal engagements.

Responsibilities

• Support development and execution of the United States Medical Affairs strategy for encaleret in ADH1 and chronic hypoparathyroidism, and support Medical Affairs launch readiness and lifecycle planning, serving as an internal medical expert with scientific rigor and patient focused decision making
• Lead integrated evidence generation planning and manage execution, including real world evidence generation, Phase 4 studies, registries, investigator initiated research support, and data integration activities
• Lead an omnichannel Health Care Professional engagement strategy, integrating field and digital scientific exchange to gather insights and inform internal Medical Affairs programs
• Build and sustain strategic relationships with key opinion leaders, investigators, and external stakeholders across endocrinology, nephrology, and related specialties, and lead advisory board and expert panel planning and execution
• Partner with Clinical Development to support ongoing and planned clinical trials and contribute to scientific data disclosure and publication strategy development in collaboration with Scientific Communications
• Provide medical leadership for peer to peer scientific exchange and external education programs, including scientific presentations and representation at scientific congresses, clinical meetings, and external forums
• Serve as medical reviewer and approver for medical, commercial, and patient advocacy materials, and support patient finding initiatives and Field Medical strategy and training in partnership with cross functional stakeholders, ensuring compliance with applicable regulations and internal Medical Affairs policies

Qualifications

• Required: MD, DO, PharmD, PhD, or equivalent advanced scientific or clinical degree
• Required: 7+ years of experience in Medical Affairs, Clinical Development, or related roles within the biopharmaceutical industry and/or academic medicine
• Preferred: Deep experience in endocrinology, rare diseases, or metabolic disorders
• Required: Demonstrated experience supporting late-stage development, launch preparation, and post-marketing medical activities
• Required: Strong scientific and clinical acumen with the ability to translate complex data into clear medical insights
• Required: Proven leadership and influence in cross-functional, matrixed environments
• Required: Excellent written and verbal communication skills
• Required: Strong understanding of regulatory and compliance requirements impacting Medical Affairs and field activities
• Required: Ability to work independently in a fast-paced, evolving organization
• Required: Strategic mindset with hands-on execution capability

Skills

• Cross-functional collaboration and leadership
• Scientific communication and publication planning
• Regulatory and compliance literacy related to Medical Affairs
• Strategic thinking with practical execution

Education

• MD, DO, PharmD, PhD, or equivalent advanced scientific or clinical degree

Additional Requirements

• Remote or hybrid/on-site work allowed (San Francisco Bay Area); travel up to ~40% for scientific meetings, advisory boards, and internal engagements