Chief of Staff for Chief Regulatory Officer (Washington)
Mavericks Wanted 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. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. Who You Are The Chief of Staff reports directly to the Chief Regulatory Officer (CRO) of BridgeBio. The Office of the CRO (OCRO) spans four pillars—Regulatory Affairs, Portfolio Strategy & Management, R&D Business Operations, and Policy & Advocacy—and this role sits at the center of all of them. The primary objective is to increase the leverage of the CRO, facilitate interactions and information flow across the OCRO and the broader BridgeBio executive leadership team, prepare materials for company leadership and the Board of Directors, take on key cross‑functional strategic initiatives, and serve as a strategic thought partner to the CRO. This role is inherently flexible, taking a central role in whatever is most critical to the OCRO at any given moment. With three NDA submissions before the FDA, a robust pipeline advancing behind them, and a policy and advocacy agenda that is growing in scope and visibility, the OCRO is operating at full throttle. The person in this role will be responsible for organizing, interpreting, and presenting a large volume of complex information—and helping the CRO and OCRO leadership use it to make better, faster decisions. They will help address urgent situations, put out fires, and put in place the processes that allow the OCRO to operate seamlessly across four distinct but deeply interconnected functions. The Chief of Staff should be: Patient‑focused A clear and structured communicator who distills complexity into concise insights and recommendations—whether the topic is a regulatory strategy, a pipeline trade‑off, an operational challenge, or a policy engagement Comfortable operating in ambiguity and able to create clarity where none exists Influential without formal authority, able to align senior stakeholders and drive follow‑through across the OCRO’s four pillars and beyond Highly emotionally intelligent, with a proven ability to handle sensitive information and confidential matters with discretion Detail‑oriented but never losing sight of enterprise‑level priorities Biased toward action, with a strong sense of ownership and accountability Resilient and adaptable, able to shift gears quickly as priorities evolve across a genuinely wide remit Responsibilities Help define and lead strategic initiatives across OCRO’s four pillars: Regulatory Affairs, Portfolio Strategy & Management, R&D Business Operations, and Policy & Advocacy Ensure cross‑functional alignment and harmonization of strategy with operational activities across the OCRO and with other functions and affiliates throughout BridgeBio Organize, interpret, and synthesize complex inputs into clear insights, recommendations, and decision‑ready materials, including succinct presentations for the CRO, OCRO leadership, senior executives, external stakeholders, and Board‑level forums Manage the operating rhythm of the Office of the CRO by setting agendas, preparing pre‑reads, tracking actions, escalating risks, and driving cross‑functional follow‑through Conduct regular reviews of case studies and literature on best practices relevant to the OCRO’s scope Manage key meetings with senior leaders across BridgeBio Question assumptions and challenge how things are done across BridgeBio in service of the patient mission Respond to urgent issues and help coordinate cross‑functional efforts Perform other strategic analyses and projects as needed True expert in the use of AI tools (Claude, ChatGPT), Excel, and PowerPoint Where You’ll Work In‑person work is a requirement for 3‑4 days per week. The role is based in our Washington DC office with some time spent in offices in Palo Alto, CA and San Francisco, CA Domestic and international travel is expected when required What It Means to Be a BridgeBio Team Member Patient Champions, who put patients first and uphold strict ethical standards Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset Truth Seekers, who are detailed, rational, and humble problem solvers Individuals Who Inspire Excellence in themselves and those around them High‑quality executors, who execute against goals and milestones with quality, precision, and speed Education, Experience & Skills Requirements Passion for delivering life‑changing treatment options into the hands of patients Familiarity with the drug discovery, development, and regulatory approval process Experience working across at least two of the OCRO’s four pillars—regulatory affairs, portfolio strategy, R&D business operations, or policy and advocacy—in a biopharma or life sciences context Proven technical and business acumen Demonstrated ability to solve problems using a structured, analytical approach Ability to handle multiple projects simultaneously Comfort working independently and as part of a diverse team Exceptional written communication and presentation skills Comfort with ambiguity and a self‑starter attitude Extremely fast learner Exquisitely detail‑oriented Highly empathetic and emotionally intelligent 3 to 6 years of relevant business development / operations / strategy experience in biopharma 2 to 3 years of experience in a top‑tier professional services firm (e.g., consulting) strongly preferred Graduate degree preferred Salary $230,000—$250,000 USD Benefits Market‑leading compensation, 401(k) with employer match, Employee Stock Purchase Program (ESPP), Pre‑tax commuter benefits (transit and parking), Referral bonus for hired candidates, Subsidized lunch and parking on in‑office days 100% employer‑paid medical, dental, and vision premiums for you and your dependents Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA) Fertility & family‑forming benefits, expanded mental health support (therapy and coaching resources) Hybrid work model with flexibility, flexible “take‑what‑you‑need” paid time off and company‑paid holidays Comprehensive paid medical and parental leave People development and internal mobility pathways—regular feedback, continuous education, and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching Performance rewards, peer‑to‑peer recognition, and growth opportunities J-18808-Ljbffr
