Jobs at Genentech

Design and build multi-agent Generative AI business applications, architect RAG-based retrieval and multimodal systems, collaborate with product and infrastructure teams to align UX and capabilities, drive observability and performance optimization, ensure regulatory compliance, mentor stakeholders, and influence technical priorities across the enterprise.

Lead prototyping and scaling of AI-driven, multi-agent and knowledge-graph solutions for real-world and clinical data. Design scalable data pipelines for unstructured and multi-modal sources, run innovation pilots, develop low/no-code analytics platforms, ensure governance and compliance (HIPAA/GDPR), and mentor teams while partnering across science, engineering, and product functions.

Lead product strategy and adoption for data-driven omnichannel orchestration and automation. Define roadmaps, business requirements, and channel prioritization logic; partner with data, analytics, technical PMs, and stakeholders to enable segmentation, audience management, decision engine integration, and feature rollouts that deliver personalized customer journeys while ensuring compliance.

Provide financial analysis and deal support for global pharma business development transactions. Drive investment decisions, build and review valuation models, manage BDFIA tools, embed AI and automation, advise on accounting implications, and coordinate cross-functional stakeholders to inform senior management and committee reviews.

Lead development and adoption of advanced statistical methodologies for clinical trials and portfolios. Provide consultation, prototype solutions (simulations, estimands, covariate adjustment), mentor staff, shape internal standards, drive external collaborations, and inform go/no-go and clinical strategy through quantitative frameworks and training.

Develop, maintain, and productionize reproducible, scalable analytical workflows and tools for bulk and single-cell transcriptomic and epigenetic data. Collaborate with computational scientists to convert analyses into reusable components, integrate multimodal data formats, and provide interfaces for scientists and downstream systems.

Lead Business Operations and Portfolio Controls for Workplace Delivery, designing and implementing enterprise systems, standardized processes, and governance. Oversee estimating, scheduling, cost control, risk management, digital enablement (dashboards, analytics, BIM integration), procurement alignment, and business services to ensure disciplined execution of large campus projects and programs.

Lead Genentech's Workplace Strategy & Design Studio to define enterprise workplace vision, technical standards, interior and lab design, and furniture strategy. Oversee lab planning, automation and robotics integration, change initiatives, and stakeholder alignment across campus and satellite sites while managing design teams, budgets, and A/E consultants.

Lead Genentech's Workplace Delivery Project Management organization, setting strategy and standards, managing ~150 capital projects across campus, ensuring scope, budget, schedule, quality, safety, compliance, and stakeholder/governance engagement while developing PM talent and organizational capabilities.

Provide strategic legal advice supporting pharma R&D (research through clinical trials) including drug/biologics/devices, AI use, data privacy, real-world data, data sharing, and human subject protection; draft and negotiate complex research and data agreements; develop guidance, templates and training; collaborate with internal global legal and business stakeholders.

Provide statistical support across clinical development and translational/exploratory projects using multimodal data. Design studies, draft SAPs, perform hands-on analyses, support CSRs and regulatory submissions, and collaborate on cross-functional teams while applying modern statistical and ML methods and maintaining scientific rigor under senior guidance.

Lead human factors engineering for combination product drug delivery devices, conducting ethnographic and usability research, use-related risk analysis, formative and summative studies, and developing instructions for use and training. Collaborate with device engineering, regulatory, clinical, quality, marketing, and program teams, define project HF activities, supervise or guide staff, and produce technical study protocols, statistical analyses, and usability reports to ensure safe, effective, and user-centered products.

Support development, scale-up, and technology transfer of parenteral drug product processes (filling, lyophilization, freeze/thaw, filtration, mixing, sterilization). Design small-scale models, run lab and pilot studies, author/approve technical and regulatory documents, troubleshoot processes, and collaborate cross-functionally with formulation, device, quality, regulatory, and manufacturing teams.

Support and manage the campus biosafety program and IBC operations. Review and approve protocols, conduct post-approval monitoring and inspections, advise researchers on regulatory compliance, manage medium-risk EHS programs, prepare committee materials and reports, and collaborate cross-functionally to resolve complex biosafety and EHS issues.

Provide regulatory support and lead Commercial Medical Legal Regulatory Review Committees (CMLRs) for assigned products. Interpret and apply FDA and Roche policies to develop and approve promotional and disease-state materials, support FDA correspondence, advise commercial leadership on marketing strategy and labeling, and manage compliance, audits, and cross-functional regulatory activities.

Lead and oversee occupational hygiene programs (industrial hygiene, biosafety, radiation, chemical safety) across the South San Francisco campus. Provide strategic leadership, ensure regulatory compliance, advise senior leadership, develop multi-year risk mitigation strategies, lead inspections, and manage and develop a team of occupational hygiene professionals.

Lead and coordinate multidisciplinary drug development programs from late research through proof-of-concept. Maintain integrated schedules and budgets, manage risks, facilitate cross-functional decisions, document program activities, and drive process improvements to meet program objectives and timelines.

Lead Clinical Scientist develops and executes early clinical development plans, authors and reviews protocols and study documents, conducts medical and protocol deviation review, answers protocol inquiries, and collaborates cross-functionally on data presentation and regulatory documentation support.

Lead global integrated lifecycle strategy and cross-functional teams for RAS portfolio from research through commercialization. Drive long-term vision, asset value maximization, resource planning, evidence generation, indications/formulations/diagnostics strategy, and alignment with development, technical, commercial, and external partners to deliver on milestones and financial targets.

The Senior Statistician leads statistical input and analysis for clinical trials, ensuring compliance and scientific rigor, and interprets results for decision-making.