Biostatistics Director, Medical Affairs

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

At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.

Salary$222,300—$255,000 USD

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.

For Full-Time U.S Based Roles

Financial & Rewards

Market-leading compensation

401(k) with employer match

Employee Stock Purchase Program (ESPP)

Referral bonus for hired candidates

Subsidized lunch and parking on in-office days

Health & Well-Being

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)