Associate Director, Biostatistics
November 23
Description
• Associate Director, Biostatistics responsible for statistical activities supporting clinical trials • Contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans • Reviewing and interpreting the analysis of clinical trial data • Interacting with internal and external cross-functional study teams • Supporting interactions with Health Authorities globally • Managing contract research organization (CRO) programmers and statisticians
Requirements
• Ph. D. in statistics or biostatistics and 5+ years relevant experience in the pharmaceutical/biotechnology industry or MS in Biostatistics or Statistics and 8+ years relevant experience in the pharmaceutical/biotechnology industry • Proven knowledge and expertise in statistics and its applications to clinical trials • Team player with the ability to work successfully across functions • Demonstrated written and excellent communication and interpersonal skills, with the ability to translate statistical concepts into layman's terms • Demonstrated leadership skills • Proficiency with statistical programming in SAS and/or R • Knowledgeable in CDISC standards, including SDTM, ADaM • Familiar with ICH guidelines, FDA, and other regulatory authority guidance • Preferably NDA experience, including eCTD submission
Benefits
• Patient Days, hearing from individuals living with conditions we impact throughout the year • A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, let science speak • An unyielding commitment to always putting patients first. Learn more about how we do this here • A decentralized model enables our program teams to focus on advancing science and helping patients • A place where you own the vision – both for your program and your career path • A collaborative, fast-paced, data-driven environment to inspire performance • Access to learning and development resources to help you get in the best professional shape • Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs) • Flexible PTO • Rapid career advancement for strong performers • Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas • Partnerships with leading institutions • Commitment to Diversity, Equity & Inclusion
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