Manager, Biostatistics

Tempus AI

1d•Remote

About The Position

Passionate about precision medicine and advancing the healthcare industry? Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

Requirements

Ph.D. or Masters Degree in Biostatistics, Statistics, or a related field with 4+ years (Ph.D.) / 6+ years (MS/MA) relevant industry experience.
Demonstrated expertise in advanced statistical analysis methods, experimental design, and survival analysis, with strong business domain knowledge in oncology, cardiology, and/or genomics.
Proven ability to improve or extend standard statistical design and analysis methods to address project-specific challenges.
Experience developing and reviewing statistical analysis plans (SAPs) and independently running analyses for complex studies with minimal oversight.
Proficiency in R and other relevant statistical software, with experience in code review and validation.
Excellent communication, organizational, and problem-solving skills.

Responsibilities

Provide expert technical and strategic leadership in the design, analysis, and interpretation of complex clinical and real-world data studies, with a focus on high-impact projects.
Collaborate cross-functionally with Engineering, Clinical/Medical, Data Science, and other stakeholders to drive project success and translate research into actionable business and clinical insights.
Lead development on statistical analysis plans -sample size and power calculations, and propose accurate and efficient statistical methodologies.
Oversee and independently execute statistical analyses for studies of high complexity, proactively identifying and addressing methodological challenges and improving or extending standard methods as needed.
Provide statistical support required for any regulatory submissions.
Independent work on complex problems, and selecting and adapting novel methods as appropriate.
Collaborate in an interdisciplinary role with scientists and engineers to translate research into actionable insights for our clients.
Stay current with advances in statistical methodologies, regulatory requirements, and industry best practices relevant to clinical trials and real-world data studies.
Comply with all regulations and Company procedures.
Mentor and provide guidance to junior and senior biostatisticians, offering both high-level project leadership and detailed technical review (e.g., SAP review, code validation).