Biostatistics Director, Medical Affairs

Job description

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.

Job Title

Biostatistics Director, Medical Affairs

Job Summary

The Director of Medical Affairs Biostatistics is responsible for statistical activities in support of external‑facing scientific communication. This includes, but is not limited to, providing scientific and methodological expertise to support medical strategy, publications, and external engagements; serving as the primary point of contact between biostatistics and the Medical Affairs team; collaborating with the team in the development of publication strategy plans; maintaining and executing Supplemental Statistical Analysis Plans (SAPs); and assisting as needed with real‑world evidence‑generating requests. They interact with both internal and external cross‑functional study teams to support the scientific communication effort, and partner with unblinded biometrics study team members to deliver needed statistical output in a timely fashion.

Responsibilities

Leads the statistical and statistical programming efforts for medical publications, scientific congresses, and external collaborations

Guides statistical design and analysis for investigator‑initiated research and collaborative studies

Provides statistical input to strategic planning of publication strategy plans

Develops and maintains Supplemental SAPs

Provides guidance to Medical Affairs team on all aspects of statistical activities to ensure methodological rigor

Works collaboratively with Medical Affairs, Project Management, Translational Medicine, and other staff to meet scientific communication timelines

Provides feedback to the Medical Affairs team regarding what is and is not possible with available data and partners with the team to brainstorm creative, scientifically sound approaches to address key questions

Interacts with the team to prospectively plan publication strategies for future congresses and manuscript generation efforts

Works with the team to develop idea‑generating analyses, including ad hoc and exploratory data analyses (EDA), to inform scientific insights and evidence‑generation opportunities

Serves as the primary point of contact for Medical Affairs requests and collaborates closely with Clinical Biostatistics and Statistical Programming leads on relevant protocols

Assists as needed with Health Economics and Outcomes Research (HEOR) and real‑world evidence (RWE) evidence‑generation requests

Where You’ll Work

This is a U.S.-based remote role that will require quarterly, or as needed visits to our San Francisco Office.

Qualifications

PhD in statistics or biostatistics with 8+ years relevant experience in the pharmaceutical/biotechnology industry or MS in statistics or biostatistics with 15+ years relevant experience in the pharmaceutical/biotechnology industry

Experienced in post‑approval / Medical Affairs settings

Strong knowledge of statistical methodologies, current drug development trends, and regulatory environments

Strong analytical and problem‑solving skills; able to identify and investigate issues and causes independently and formulate potential solutions

Established publication record and experience supporting scientific communication

Able to work effectively in cross‑functional, matrixed environments

Excellent written and verbal communication skills, with the ability to engage both technical and non‑technical audiences

Excellent programming skills, including the ability to independently generate publication‑ready figures; R and/or SAS programming fluency preferred

Able to work in a fast paced environment

$222,300 - $255,000 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 to care for yourself and your family

Skill Development & Career Paths

People are part of our growth and success story—from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility

We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, & BetterUp Coaching

We celebrate strong performance with financial rewards, peer‑to‑peer recognition, and growth opportunities

As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

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Worksite address

san francisco, CA, 94199, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.