88- 50100571 Data Scientist

Roche • South San Francisco, CA

13d • Hybrid

About The Position

Genentech, Inc. seeks a Data Scientist at its South San Francisco, California location. Duties: Within medical diagnostic industry, provide statistical analysis and leadership on cross-functional teams to shape clinical development strategies for new molecular entities. Apply expertise in theoretical and applied statistics and programming within a collaborative environment to develop and review clinical study protocols. Oversee trial progress, ensuring timely delivery of analyses to inform clinical development decisions. Contribute to regulatory/government submissions, including clinical protocols, study reports. Offer consulting and guidance on exploratory data analysis, including biomarkers, pharmacokinetics, and pharmacodynamic data, and provide training on statistical methods. Collaborate with scientists to conduct key analyses and create data visualizations for scientific conferences and publications.

Requirements

• Master’s degree, or foreign equivalent, in Public Health, Statistics, Biostatistics, Mathematics, or a closely related field.
• Advanced Statistical Programming with SAS & R
• Applied Data Mining & Machine Learning
• SAS for regulatory-compliant statistical analysis in clinical trials
• Python for data wrangling, machine learning, and predictive modeling
• Data visualization to support reporting events and publications
• Engineering, data preprocessing, and dimensionality reduction to analyze complex clinical and biomarker datasets to identify patterns
• Protocol development and regulatory considerations to support statistical aspects of clinical development strategy
• Simulation-based methods, Bayesian methods, and advanced regression models to conduct robust statistical modeling.

Responsibilities

• Provide statistical analysis and leadership on cross-functional teams to shape clinical development strategies for new molecular entities.
• Apply expertise in theoretical and applied statistics and programming within a collaborative environment to develop and review clinical study protocols.
• Oversee trial progress, ensuring timely delivery of analyses to inform clinical development decisions.
• Contribute to regulatory/government submissions, including clinical protocols, study reports.
• Offer consulting and guidance on exploratory data analysis, including biomarkers, pharmacokinetics, and pharmacodynamic data, and provide training on statistical methods.
• Collaborate with scientists to conduct key analyses and create data visualizations for scientific conferences and publications.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level