Jobs at Genentech

Lead the strategy, development, and lifecycle management of pharmaceutical forecasting products and platforms. Translate pharma revenue forecasting expertise into scalable analytical solutions, partnering with data science, AI/ML, IT, finance, and commercial stakeholders. Oversee requirements, roadmap execution, process mapping, UAT, agile backlog management, launches, adoption, and optimization. Drive stakeholder alignment, executive communication, compliance, and coaching across cross-functional product teams.

Lead a centralized administrative function of ~70 professionals supporting 3,000 scientists. Define organizational design and strategic vision, partner with executives on operational effectiveness, implement modern training and AI-enabled tools, manage staffing and budgets, drive inclusion and career development, and foster a high-performing administrative community aligned with scientific goals.

Leads global legal spend management, governance, analytics, budgeting, pricing negotiations, law firm panel management, and Alternative Legal Service Provider integration. Oversees e-billing and matter management system adoption, modernizes legal pricing models, evaluates external counsel and LegalTech partners, and develops data-driven vendor management practices. The role manages large global budgets, builds international teams, influences senior stakeholders, and drives technology-enabled efficiency across legal and compliance divisions.

Performs biostatistical analyses supporting clinical trials, translational research, and exploratory initiatives across pharmaceutical development. Responsibilities include study design, protocol development, statistical analysis plans, clinical study reports, multimodal data analysis, predictive modeling, and regulatory submissions. The role collaborates with cross-functional teams, applies statistical and machine learning methods, communicates findings, and maintains analytical quality under senior guidance.

Six-month, on-site internship supporting pharmaceutical technical development through digital science projects. Responsibilities include building data-processing workflows, visualization dashboards, software applications, databases, and data science models; analyzing mass spectrometry data; benchmarking analytical platform performance; and improving data extraction and processing throughput. Interns present projects to senior leaders and participate in professional development and program activities.

Leads organized customer access marketing strategy for a lymphoma product launch and existing portfolio. Develops omnichannel campaigns, customer strategies, compliant promotional content, EHR orderset initiatives, contracting support, agency partnerships, field deployment, measurement plans, and campaign optimization across payers, providers, GPOs, financial decision makers, and patients. Partners cross-functionally with pricing, contracting, distribution, legal, regulatory, medical, government affairs, and marketing teams.

Leads GPCR pharmacology and drug candidate characterization from early research through IND selection. Develops and optimizes biochemical and cellular assay cascades, investigates receptor mechanisms, analyzes complex datasets, guides multidisciplinary project decisions, mentors scientists, evaluates emerging technologies, and communicates findings to project teams and senior leadership.

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.

Leads digital transformation of pharmaceutical regulatory workflows through AI and data strategy. Drives cross-functional initiatives, process redesign, innovation, compliance, stakeholder engagement, and enterprise change. Serves as a subject matter expert, mentors colleagues, builds organizational capabilities, and manages complex projects involving internal teams, health authorities, government entities, and external stakeholders.

Develops antibody- and therapeutic-molecule-expressing CHO cell lines for clinical and commercial manufacturing. Responsibilities include executing cell line development experiments, improving targeted integration efficiency, streamlining platform processes, analyzing gene copy numbers, and working independently across parallel studies. The role requires strong molecular and cell biology expertise, communication and presentation skills, collaboration, and problem-solving in an on-site South San Francisco research environment.

Conduct biochemical and cellular pharmacology research for cardio-metabolic drug discovery. Design and execute biochemical and cell-based assays, characterize therapeutic candidates, investigate receptor signaling and protein interactions, develop novel assay platforms, and support screening across multiple projects. Use laboratory automation, analyze complex data, document findings, and communicate results across multidisciplinary teams.

Leads risk-based quality strategies, audits, issue management, quality conclusions, and compliance activities across GCP, pharmacovigilance, personalized healthcare, and computerized systems. Oversees service provider quality, supports health authority inspections, develops procedures, and leads global cross-functional initiatives. The role also provides expert guidance, mentorship, and regulatory compliance support across Roche and Genentech.

Leads enterprise-wide pharmaceutical R&D digital and data initiatives from strategy through operationalization. Translates complex business needs into product roadmaps, capabilities, and priorities while coordinating cross-functional teams, vendors, architects, engineers, and data scientists. Evaluates AI, machine learning, analytics, APIs, and modern data platforms for strategic fit and scalability. Manages executive stakeholders, drives decisions in ambiguous environments, mentors colleagues, and shapes R&D technology and workforce strategies.

Interns support biopharmaceutical process development through wet-lab, dry-lab, and digital experiments involving purification, microbiology, virology, process optimization, analytical methods, data analysis, and automation. Projects may address downstream processing, viral clearance, protein stability, impurity removal, filtration, assay workflows, and AI-enabled analysis. Interns collaborate with scientists and engineers on business-critical projects and present results to senior leaders.

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.

Provides strategic legal counsel to Roche’s pharmaceutical R&D functions across research, clinical operations, product development, medical affairs, AI, data privacy, and human-subject protections. Drafts and negotiates research collaboration and data-sharing agreements with external partners, develops legal guidance and training materials, and collaborates with global legal, regulatory, ethics, scientific, and business stakeholders. The role requires advanced knowledge of FDA, healthcare fraud and abuse, privacy, and human therapeutics regulations.

Leads the strategic vision and operational framework for companion diagnostic development, clinical platforms, and biomarker policy innovation. Oversees assay and platform development across established and emerging technologies, regulatory strategy, diagnostic partnerships, and Health Authority engagement. Builds cross-functional alignment across pharmaceutical, diagnostics, clinical, regulatory, commercial, and medical teams. Manages and mentors 6–8 scientific professionals, setting priorities, budgets, talent strategies, and operational plans to advance precision medicine and therapeutic development.

Lead research projects investigating T-cell biology and immunoregulatory mechanisms, identify and validate therapeutic targets for inflammatory diseases, generate proof-of-concept data, design complex cellular and animal experiments, and collaborate across genetics, biomarker discovery, and early clinical development teams.

The role involves developing AI models to enhance clinical trials by connecting molecular data with clinical outcomes and supporting decision-making processes in drug development.

Conducts in vivo experiments in rodent models of cardiovascular and cardiometabolic diseases to support drug discovery. Responsibilities include developing disease models, performing survival surgeries, administering compounds, collecting blood and tissues, phenotyping animals, analyzing experimental data, maintaining reproducible ELN records, and presenting findings to multidisciplinary teams. The role requires strong cardiovascular model expertise, including myocardial infarction, ischemia-reperfusion, transverse aortic constriction, echocardiography, and heart catheterization.