This position is based in South San Francisco, on site.

The Opportunity

The Biostatistician will work across diverse therapeutic areas including Ophthalmology, Cardiovascular, Renal, and Metabolism (CVRM), and Immunology portfolios, contributing to projects at the intersection of statistics, data science, and clinical development. In this dynamic role, you will balance support for core clinical trial operations with translational research. You will assist in providing statistical input and hands-on execution for both traditional studies and complex exploratory initiatives, utilizing multimodal data – including biomarkers, imaging, and digital health measurements – to advance high-value work and inform molecule-level development decisions.

As a statistical partner within cross-functional teams, you will help ensure scientific rigor and analytical excellence. You will support the analysis of diverse and complex datasets, apply established methodologies, and help build the evidence required to support strategic decision-making and global regulatory submissions.

Your Responsibilities

• You contribute to the statistical execution and analytical strategy for a diverse portfolio of work, ranging from clinical study deliverables to translational and exploratory initiatives under guidance, ensuring scientific integrity across all deliverables.
• You perform or support hands-on analysis of multimodal data, researching and applying statistical methodologies and predictive modeling to address clinical challenges, escalating issues when needed.
• You support statistical execution for traditional clinical trials under guidance, which includes assisting with study design, protocol development, drafting Statistical Analysis Plans (SAPs), and supporting Clinical Study Reports (CSRs) for regulatory submissions.
• You participate as a statistical team member on cross-functional teams, helping to translate complex data into clear communications and actionable insights with support from senior colleagues.
• You represent Biostatistics and PDD on cross-functional project teams, ensuring the statistical rigor of study deliverables under guidance.
• You maintain up-to-date knowledge of the latest developments within the fields of statistics, machine learning, and data science to ensure the application of appropriate analytical approaches.
• You apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations.
• You adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological expertise.

Who You Are (Required)

• You hold a PhD or MSc in Statistics, Biostatistics, Machine Learning, or a closely related quantitative discipline.
• You have 0-2 years of relevant experience in clinical trial statistics or applied data science within a pharmaceutical, biotech, or CRO setting.
• You possess an understanding of statistical principles and methodology relevant to the analysis of multimodal data to drive data-informed decision-making.
• You are proficient in programming using R, Python, and/or SAS to solve analytical problems.
• You demonstrate capacity for independent thinking and the ability to make decisions based upon sound principles.
• You have excellent verbal and written communication skills, with the ability to summarize findings clearly and explain technical concepts to diverse stakeholders with support from senior colleagues.
• You thrive in a global environment, demonstrating respect for cultural differences and the ability to work effectively within a matrixed team structure.

Preferred

• Experience in at least one specialized data domain: biomarkers, imaging, or digital health measurements.
• Experience or academic background in translational and exploratory analyses.
• Familiarity or academic knowledge of operating as a study-level statistician, including regulatory guidelines (e.g., ICH), CDISC standards, and standard clinical trial deliverables.
• Knowledge of multiple drug development phases (early and late stage), clinical trial design, and an understanding of the broader pharmaceutical industry context.
• Experience working in cross-functional or scientific project teams.

Relocation benefits are not available for this posting.

The expected salary range for this position based on the primary location of California is 120 800,00 - 224 400,00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.