Director/Senior Director of Managed Access

Confirmed live in the last 24 hours

BridgeBio Pharma

Palo Alto - 3160 Porter

Hybrid

Posted March 27, 2026

Job Description

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.

What You'll Do

The Director/Senior Director of Managed Access will help shape the strategy and operations of the BridgeBio Managed Access Program, which seeks to provide our medicines to patients in countries where we are not pursuing commercial efforts. BridgeBio’s objective function is to provide as many new and meaningful drugs that have a profound impact on as many patients as possible, which includes an imperative to create sustainable and efficient pathways to delivering our medicines around the world. This role is cross-functional and will coordinate efforts across groups within BridgeBio including Management, International, Medical, Regulatory, Supply, Quality, Pharmacovigilance, Legal, Finance, Commercial, and others. The role will be external facing and will interface with stakeholders including patients, physicians, partners, vendors, regulatory bodies, media, and others.

Responsibilities

Help define/lead the strategic design and implementation of the program
Ensure cross-functional alignment and harmonization of strategy with operational activities
Evaluate external partnership opportunities to grow and scale the program
Manage vendors supporting the initiative
Coordinate the internal cross-functional working group and governance committee
Project manage the intake and evaluation process for new patient requests
Manage and refine the budget
Question assumptions and challenge how things are done in service of the patient mission
Respond to urgent issues
Support the interface with external parties including patients, physicians, partners, vendors, regulatory bodies, media, etc.

Where You'll Work

In-person work is a requirement in both our Palo Alto and San Francisco, CA offices
Domestic and international travel is expected when required

Who You Are

Passion for delivering life-changing treatment options into the hands of patients
Motivation to create access to medicines in low- and middle-income countries (LMICs)
Familiarity with the drug discovery & development process
Proven scientific and business acumen
Demonstrated communication skills and an ability to distill complexity into concise insights and recommendations
Comfort operating in ambiguity and able to create clarity where none exists

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