Lead federal policy strategy to influence national debates on drug development and patient access as a trusted representative for BridgeBio.
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma.
This role is a core member of BridgeBio’s Policy & Advocacy team, a highly collaborative function that works across scientific, regulatory, commercial, patient advocacy, and communications units to anticipate policy risks and shape opportunities that impact BridgeBio’s pipeline and patient communities. The Director will be responsible for building and sustaining trusted relationships with lawmakers, committee staff, and aligned stakeholders, ensuring BridgeBio is positioned as a credible and influential stakeholder.
The Director will anticipate and interpret legislative and policy developments, translating federal policy shifts into strategic guidance that informs enterprise planning and pipeline strategy. They will advise senior leadership and inform enterprise decision-making to support senior executives, program leaders, and affiliate organizations as they engage in matters affecting drug development, rare disease therapies, oncology innovation, and market access. The Director will help shape the company’s federal political engagement strategy, ensuring alignment with BridgeBio’s long-term scientific and policy objectives.
The Director will embody BridgeBio’s science-driven, entrepreneurial culture in advancing its federal policy priorities.
The ideal candidate is an experienced, strategic legislative or government affairs professional with a deep understanding of the federal policy environment shaping drug development, biomedical innovation, and patient access. This individual brings a proven track record of building trusted, influential relationships across Congress, federal agencies, and the broader health policy ecosystem. They are energized by complex, evolving policy challenges and know how to translate those challenges into actionable strategies that advance organizational priorities.
Federal Government Affairs Strategy
Relationship-Building & Stakeholder Engagement
Policy Analysis, Forecasting & Translation
Cross-Functional Collaboration & Influence
Strategic Communication & Executive Support
Mission Orientation & Patient-Centered Advocacy
This is a hybrid role based in Washington, D.C., requiring regular in-office collaboration and in-person engagement with policymakers and stakeholders.
We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
Financial Benefits:
Health & Wellbeing:
Skill Development & Career Paths:
Health Insurance
Comprehensive health care with 100% premiums covered - no cost to you and dependents
401K employer match
Employer match on 401K with 100% on first 3% & 50% on the next 2%
Paid Parental Leave
Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents
Paid Time Off
Unlimited flexible paid time off - take the time that you need
BridgeBio Pharma is a biopharmaceutical company focused on discovering and delivering transformative medicines for genetic diseases and genetically defined cancers. Utilizing a 'moneyball for biotech' approach, we minimize risk and drive innovation through small expert teams, creating a robust portfolio of over 20 drug development programs to address unmet medical needs.
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Director Q&A's