BridgeBio Pharma
Executive Director, Scientific & Medical Excellence
Remote - USA · Director · Full-time
Sponsorship not specified$279k-$330kDetected 8 days ago
Data ScienceA/B TestingSupply ChainResearchLeadershipCommunicationPublic Speaking
About the role
- Mavericks Wanted When was the last time you achieved the impossible?
- Together we define white space, push boundaries, and empower people to solve problems.
- Together, we'll ask "why not?" and help reengineer the future of biopharma.
Responsibilities
- Ensure evidence plans support regulatory interactions, value demonstration, payer engagement, and HTA requirements, and that data are disseminated through a coordinated publication strategy.
- Develop and manage sponsored research collaborations and external research partnerships with academic centers, consortia, and cooperative groups.
- Partner with Legal, Compliance, Finance, and Regulatory to ensure all externally sponsored research meets internal standards and applicable regulations.
- Partner with Regulatory, Clinical, Supply Chain, Legal, and Patient Advocacy across regions to ensure consistent, equitable, and compliant access processes.
- Partner with Data Science, IT, Legal, and Compliance to establish responsible-use, governance, validation, and data-privacy guardrails for AI tools in a regulated environment.
- Champion change management and capability building so teams adopt new tools effectively, with measurable impact on quality, speed, and decision-making.
Requirements
- MD, DO, PharmD, PhD, or equivalent advanced scientific or clinical degree.
- High degree of scientific rigor, integrity, and patient-centered focus.
Nice to have
- Demonstrated experience in rare disease strongly preferred.
Compensation
- $279,000 - $330,000 USD
- Market-leading compensation
Benefits
- The Executive Director, Scientific & Medical Excellence is a senior leadership role within Medical Affairs, accountable for the cross-cutting scientific capabilities and programs that serve BridgeBio's portfolio.
- This individual will build and scale the operating model, governance, and standards that allow Medical Affairs to act with scientific rigor, speed, and compliance.
- The role requires deep expertise in rare disease, the maturity to lead in a matrixed, fast-paced environment, and the vision to modernize how a medical organization generates and exchanges scientific evidence.
- The role partners closely with Clinical Development, Regulatory, Commercial, Market Access, HEOR, Patient Advocacy, and Field Medical.
- Lead the development of the integrated evidence generation plan, in partnership with HEOR, aligned to overarching medical and asset strategy and informed by clearly prioritized scientific and stakeholder evidence gaps.
- Medical Information
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