Jobs at Genentech

Lead a multidisciplinary functional genomics team to define strategy, develop large-scale screening and multi-omics capabilities, integrate emerging technologies and automation, partner across research and development functions, and build external collaborations to accelerate target identification, biomarker discovery, and drug development.

Lead toxicology safety assessment for therapeutic programs (oncology, cardio/respiratory/metabolism) by designing/supervising studies, interpreting data, preparing regulatory documents, communicating with authorities, investigating toxicity mechanisms, and mentoring team members.

Lead strategy and roadmap for 360-degree customer insight products for commercial and medical teams. Own product lifecycle, prioritize features, coordinate cross-functional teams (data science, IT, activation), drive enterprise integrations and APIs, ensure compliance with medical/commercial data rules, and deliver measurable business impact across channels.

Support PTQ Quality Processes by contributing to initiatives, facilitating workshops, developing metrics and data repositories, generating business insights, and assisting PTQ strategy and project management across cross-functional teams.

Lead strategy and execution for Targeting & Recommendation analytics products: define vision and roadmap, translate complex data and models into scalable products, manage full product lifecycle, partner with data science and engineering, drive cross-functional adoption, establish agile product practices, and mentor product teams while ensuring regulatory compliance.

Support coordination and delivery of virtual, hybrid, and in-person learning programs. Manage logistics, communications, attendance tracking, and learner support. Maintain project trackers, analyze learning data, create simple dashboards/reports, and help design learner materials and assessments. Research and recommend innovative learning tools and AI-enabled approaches. Improve one recurring operational process and document it for scalability.

Lead data management strategy and a team of 6-8 data managers for early-phase clinical programs. Ensure analysis-ready data, design fit-for-purpose data practices for non-standard and exploratory data, align biometrics contributors, drive process improvements, mentor staff, manage capacity and quality expectations, and represent data management across cross-functional and regulatory contexts.

The Principal Biostatistician designs and analyzes early-phase clinical trials, applying statistical expertise to inform trial strategy and regulatory interactions. Responsibilities include leading study designs, ensuring quality statistical deliverables, and shaping clinical narratives based on complex data analysis.

The Expert Imaging Lead for CVRM leads therapeutic area imaging strategies, integrating AI and ML within clinical research and drug development, collaborating with cross-functional teams and external partners for scalable imaging solutions.

The Computational Scientist will lead computer vision and AI/ML projects, develop machine learning algorithms for spatial omics data, and collaborate with researchers for data interpretation and visualization.

The Principal Quality Lead develops Quality strategies based on risk, conducts audits, addresses compliance, and mentors within the organization.

Responsible for leading marketing strategies for Neurodegeneration products, including team development and execution of strategic business plans to enhance patient outcomes and market penetration.

The role involves leading and mentoring a team in analytical development for biologics, managing projects, and supporting regulatory submissions.

The Director will lead the Specialized Analytics team in biologics development, overseeing complex analytics, driving innovation, and ensuring quality and collaboration.

Lead the design and characterization of next-generation antibody therapeutics. Collaborate across teams to analyze data and inform project decisions.

The Senior Director leads a team in analytical characterization of biologics, overseeing strategies and advancing digital efforts in a fast-paced environment.

The Senior Director leads a team in Analytical Development, overseeing strategies and deliverables for biologics, ensuring compliance and managing cross-functional collaboration while supporting regulatory submissions.

The Technical Development Principal Scientist will design and execute analytical studies for process development and regulatory filings, contributing as an analytical expert in a CMC team for clinical therapeutics.

Genentech seeks postdoctoral fellows to engage in biomedical research, develop technologies, and publish findings. Ideal candidates should have a recent Ph.D. and a first-author publication, with strong critical thinking and communication skills.

Lead the engineering team in developing integrated digital marketing solutions for Pharma, focusing on customer journey orchestration and technology platform enhancements.