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Genentech
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  • The PositionA healthier future. It’s what drives us to innovate. To co... Read More
    The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. The OpportunityThe Neurodegenerative Diseases Pipeline Medical Science Liaison (NDG Pipeline MSL) is a credible field medical partner responsible for providing clinical, scientific and other relevant information related to disease states and the appropriate utilization of Genentech medicines in the NDG pipeline. This field-based position will engage with healthcare providers, clinical study staff, therapeutic area experts (TAEs), population health decision makers, and patient thought leaders within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with home office and regional partners, NDG Pipeline MSLs are accountable for comprehensive activities focused on delivering a successful clinical development program including, but not limited to: clinical trial recruitment focused activities, competitive intelligence, congress support, professional society engagement, and therapeutic area landscaping. In addition, NDG Pipeline MSLs may be responsible for covering multiple pipeline medicines, as well as engaging in broad clinical and scientific discussions  resulting in rich customer insights shared with key stakeholders across the organization. Preferred States of ResidenceTexasOklahomaArkansasMissouri LouisianaKey ResponsibilitiesEnsure an end to end customer experience for NDG customers within the region. Demonstrate deep clinical and scientific expertise about assigned molecules/products pipeline/line of sight, franchise(s) and overall  therapeutic area(s) to exchange relevant information and insights with top tier thought leaders, clinical investigators and related staff, and healthcare decision makers within a region Build, cultivate, and leverage relationships with key external scientific and medical customers and organizations in their region(s) to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape. Develops engagement plans aligned with customer needs and preferences and global strategyEngage in continuous independent learning within the therapeutic area they represent and actively attend and participate in upskilling programs related to assigned molecules, products, disease states  and relevant business topics Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and Genentech guidelines, policies & procedures Build and cultivate important working relationships across field partners and internal stakeholders to ensure an enterprise approach when working with customers. Be accountable to the regional team to shape and execute on local medical strategies within planned timelines. Help to set and act on aligned clinical disease area priorities, and relay/flag any potential mismatch in priorities between internal stakeholders and the site as well as relay any key site-related decisions on behalf of the businessProvide Congress and conference support, facilitating engagement between HCPs and the broader Pipeline Medical Team, as appropriate, and participating in competitive intelligence, medical booth support and related activitiesIdentify and bring insights back in house to Genentech stakeholders through efficient and effective use of CRM system and cross functional collaboration.  Endorse investment decisions in PIs and/or sites to support the overall Disease Area strategy.  Help create transparency around customer needs,Assist with Phase I - IV sponsored and supported clinical trials, health economic outcomes research, other therapeutic area specific medical collaborations; provide clinical expertise overview of performance metrics and feedback regarding  operational management of clinical trials to ensure optimal site selection and performance.   Fully understands site infrastructure and ways of working to best co-create and monitor clinical trial processes.  Supports start-up, recruitment, and retention in assigned geographies. Provides critical collaboration with CRO personnel, as appropriate, and in pre-specified mannerShare clinical and value-based expertise in the development and management of clinical and  scientific communications for customers to include publications, conference data, and educational  materials, as well as for internal Genentech communications and materials to be used in training and  development activities Ensure assigned goals, objectives, and KPIs are met and that assigned projects and other work are  completed on time, with high quality, and within budget Who you areQualifications & ExperienceAdvanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.). BSN with extensive field medical experience with a pharmaceutical companyMinimum of 5 years related work experience (clinical, managed care, or industry experience)  Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.Preferred ExperiencePrior experience as a field MSLTherapeutic area experience in Alzheimer’s Disease and/or Parkinson’s Disease 2 + years’ clinical research experience (either in industry or in another, related setting)2 + years' experience in therapy areaIn-depth knowledge of clinical development programs and clinical trial managementPrior experience working in heavily matrixed organizations interfacing with clinical operations, clinical development and medical affairs organizationsLocation and Travel RequirementsBusiness travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time)This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.Applicants should reside within 30 miles of a major airport and should reside within 50 miles of the established territory. Preference will be given to applicants who reside within preferred states of residence listed above.The expected salary range for this position is $161,280 - $299,520.00.  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.BenefitsRelocation benefits are not available for this job posting.Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202602-104884Date posted : 2026-06-30Profession: Medical & Government AffairsEmployment type: Full time Read Less
  • Sr. Manager, Policy Communications  

    - San Mateo County
    The PositionThe OpportunityThe Policy Communications team within Genen... Read More
    The PositionThe OpportunityThe Policy Communications team within Genentech’s Corporate Communications department is seeking an experienced Senior Communications Manager to drive strategic communications for emerging policy issues and elevate our organization’s thought leadership among external stakeholders. The role will lead communications, issues management and execution connected to Genentech’s manufacturing footprint, capital investments, and economic development priorities.The successful candidate will serve as a trusted partner capable of collaborating across a global matrixed organization on communications for high-visibility, high-impact events and strategic initiatives. We are looking for an individual with specialized policy and public affairs expertise, a proactive mindset, and a proven track record of navigating complex political and media landscapes.Key ResponsibilitiesStrategic Communications: Work across teams to spearhead proactive policy communications, digital advocacy, and earned media campaigns for emerging issues at the federal, state, and local levels.Content Architecture: Design and maintain a suite of high-impact communications materials, including core messaging frameworks, infographics, one-pagers, and dynamic digital content.Digital Thought Leadership: Design and execute an ongoing content and editorial strategy for Genentech-owned channels to increase external visibility and showcase leadership on differentiating policy topics.Capital & Infrastructure Communications: Lead communications for Genentech's portfolio of capital investments and expansions, executing communications for high-visibility milestones and events (e.g., ribbon-cuttings, manufacturing announcements) and VIP executive site visits.Economic Impact Storytelling: Drive narrative-driven storytelling around Genentech’s regional innovation and economic investment and impact, managing targeted media relations with key local and regional reporters.California Home-State Strategy: Support the execution of a highly coordinated policy communications strategy for California, including for a major headquarters campus expansion underway in South San Francisco.Internal & Community Engagement: Manage internal and community-facing communications, including the development of internal updates, newsletters, events, and activations.Compliance: Ensure strict alignment and compliance with all applicable laws, regulations, and Genentech policies.Travel: Travel as required to support executive engagements and business priorities.Who you areYou have a Bachelor’s degree.You have 8+ years of professional communications experience,You have at least 6 years dedicated to policy communications, public affairs, or political campaigns.Demonstrated understanding of the U.S. healthcare policy and/or political landscape, with the ability to translate complex regulatory and legislative topics into compelling, accessible narratives.Experience leveraging digital platforms to advance policy priorities and elevate thought leadership.A proven track record of designing and executing high-impact communication strategies in collaboration with diverse, cross-functional internal and external teams.Hands-on experience leading communications for major corporate or political milestones, including on-the-ground event execution and direct, proactive engagement with reporters.Exceptional writing and editing skills under tight deadlines, with a forward-thinking ability to leverage AI and digital tools to drive efficiency and support a best-in-class communications function.Experience managing external communications agencies, vendor contracts, and complex project budgets simultaneously.Preferred QualificationsAdvanced degree in a relevant field.Proven track record in pharmaceuticals, biotechnology, or another highly regulated sector. Experience within a trade association or communications agency is highly desirable.Experience managing sustainability and economic development issues is a plus.Experience driving and advancing strategic communications within a complex, global organization.Exceptional skills in launching and managing complex, large-scale, cross-functional initiatives involving both internal and external stakeholders.Location & Travel RequirementsBased onsite in Washington, D.C. or South San Francisco, CA.Domestic travel on an as-needed basis to manufacturing sites and for milestone events is required.Relocation benefits are NOT offered on this posting.The expected salary range for this position based on the primary location of Washington DC is $120,800/yr to $224,400/yr. 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.Benefits#LI-CM4Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202607-117525Date posted : 2026-07-23Profession: Business Strategy & DeliveryEmployment type: Full time Read Less
  • Head, Resourcing & Metrics  

    - Suffolk County
    The PositionA healthier future. It’s what drives us to innovate. To co... Read More
    The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.This role is based in Business Strategy & Operations (BSO) which serves as the strategic backbone and operational enabler for Product Development Data Sciences (PDD). The function ensures organizational excellence through robust quality frameworks, optimized resourcing, and aligned strategic execution. BSO brings together cross-functional capabilities across quality and compliance, workforce planning, and strategic operations to empower leaders and teams to deliver with focus, transparency, and accountability. By connecting enterprise priorities with operational realities, BSO drives consistency, clarity, and coordinated progress across PDD and the broader development organization.The Opportunity: The Head of Resourcing & Metrics within the Business Strategy & Operations (BSO) function is accountable for overseeing enterprise-wide resourcing, budget tracking, and impact measurement strategies across Roche’s PDD portfolio. This role provides leadership in resource planning, workforce analytics, and metrics-driven performance management, supporting senior functional leadership in data-informed decision-making. The Head of Resourcing & Metrics plays a critical role in ensuring organizational agility, financial transparency, and operational excellence, and maintains strong partnerships with Finance, HR, and other enabling functions.You provide strategic direction for a team of leaders responsible for designing and driving the oversight and management of resourcing and financial tracking to ensure accurate visibility into headcount, contractor usage, and financial allocations across all functions and geographiesYou drive end-to-end planning governance across PDD in partnership with Finance, HR, Portfolio, and other enterprise stakeholders, ensuring consistent standards, data integrity, and transparent accountabilityYou drive various cross-functional and partnership governances to bring the R&M team and stakeholders together to maintain a single source of truth for financial and resourcing performance and enable executive decision-making and resource optimizationYou engage heavily with your direct team and stakeholders, and also with leadership — specifically with the Head of BSO and Head of PDD — to ensure high-quality, data-driven, and proactive insightsYou lead your direct team to develop and execute departmental plans to ensure alignment with business and organizational prioritiesYou shape and govern enterprise-aligned metrics frameworks (e.g., OKRs, KPIs) that measure the performance, productivity, and strategic impact of BSO and other PDD functionsYou lead multi-year planning and quarterly forecasting processes, ensuring alignment of headcount and budget forecasts with evolving portfolio and business prioritiesYou establish and oversee cross-functional operating rhythms that ensure the alignment of resource data with program timelines, study demand, and investment trade-offsYou set strategic direction for data governance, audit compliance, and quality controls related to resource and budget information, ensuring accuracy, traceability, and alignment with Roche policiesYou influence enterprise-wide workforce planning efforts by delivering robust analytics, capacity modeling, and actionable insights to senior leadershipYou identify and drive innovation opportunities in automation, analytics tooling, or enterprise planning systems (e.g., Anaplan, Tableau, Adaptive Insights) to increase planning efficiency and qualityYou lead and develop a multi-layered team of leaders, resource planners, financial analysts, and metrics experts across diverse geographiesYou ensure appropriate team structure, skill mix, and capacity to deliver strategic priorities and day-to-day operational excellence in a dynamic and fast-paced business environmentYou provide coaching and leadership development to direct reports, empowering them to operate autonomously and thrive in an evolving business environmentYou set clear expectations and accountabilities for excellence in planning, analysis, stakeholder engagement, and cross-functional collaborationYou represent the BSO function in enterprise-level forums and negotiations related to budget, workforce, and investment prioritizationYou act as a thought partner to the Head of BSO and PDD LT on operational and strategic decisions related to planning, performance, and resource optimizationYou balance operational delivery with longer-term capability-building, ensuring that BSO evolves in line with future business needs and industry standardsWho you are:You have an advanced degree in Business, Finance, Data Analytics, Organizational Strategy, or a related field (preferred)You have 15+ years of progressive experience in business operations, enterprise planning, or resource and financial governanceYou have 6+ years in senior leadership roles, including managing senior professionals or people leaders across functions and locationsYou have proven success in driving resource planning and analytics strategy across complex, matrixed organizations, ideally in life sciences, R&D, or healthcareYou have demonstrated ability to lead large cross-functional initiatives with high organizational impact and visibilityYou are proficient with enterprise planning and reporting tools (e.g., Anaplan, PowerBI, Tableau) and financial modeling for large-scale functionsYou have strong stakeholder management and influencing skills, including experience engaging with senior executives and enterprise leadershipYou have capacity for independent thinking and ability to make decisions based upon sound principlesYou exhibit excellent strategic agility including problem-solving and critical thinking skills, and agility that extends beyond technical domainYou demonstrate respect for cultural differences when interacting with colleagues in the global workplaceYou possess excellent verbal and written communication skills, specifically in the areas of presentation and writing, with the ability to explain complex technical concepts in clear languagePreferred Qualifications:Familiarity with Roche’s PDD or PD organizational structure and planning processesExperience designing and implementing metrics frameworks or impact measurement strategies in scientific or technology-driven environmentsTrack record of embedding planning best practices and building scalable operations in global teamsDeep understanding of the interplay between portfolio governance, workforce strategy, and enterprise financial cyclesDemonstrated success in aligning operational resources to scientific, digital, or innovation-led prioritiesRelocation benefits are not available for this postingThe expected salary range for this position based on the primary location of California is $201,300.00 - $373,800.00.  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.Benefits#PDDT#PDDSSFGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202509-124588Date posted : 2026-07-09Profession: Business Strategy & DeliveryEmployment type: Full time Read Less
  • The PositionA healthier future. It’s what drives us to innovate. To co... Read More
    The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. The OpportunityThe Metabolic dysfunction-associated steatohepatitis (MASH) Pipeline Medical Science Liaison, a part of the Cardiovascular, Renal and Metabolism (CVRM) MSL team, is a credible field medical partner responsible for providing clinical, scientific and other relevant information related to disease states and the appropriate utilization of Genentech medicines in the MASH pipeline. This field-based position will engage with healthcare providers, clinical study staff, therapeutic area experts (TAEs), population health decision makers, and patient thought leaders within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with home office and regional partners, MASH Pipeline MSLs are accountable for comprehensive activities focused on delivering a successful clinical development program including, but not limited to: clinical trial recruitment focused activities, competitive intelligence, congress support, professional society engagement, and therapeutic area landscaping. In addition, MASH Pipeline MSLs may be responsible for covering multiple pipeline medicines, as well as engaging in broad clinical and scientific discussions  resulting in rich customer insights shared with key stakeholders across the organization. Preferred States of Residence• Alabama• Florida• Georgia• Mississippi• North Carolina• South Carolina• TennesseeKey ResponsibilitiesEnsure an end to end customer experience for MASH customers within the region. Demonstrate deep clinical and scientific expertise about assigned molecules/products pipeline/line of sight, franchise(s) and overall  therapeutic area(s) to exchange relevant information and insights with top tier thought leaders, clinical investigators and related staff, and healthcare decision makers within a region Build, cultivate, and leverage relationships with key external scientific and medical customers and organizations in their region(s) to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape. Develops engagement plans aligned with customer needs and preferences and global strategyEngage in continuous independent learning within the therapeutic area they represent and actively attend and participate in upskilling programs related to assigned molecules, products, disease states  and relevant business topics Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and Genentech guidelines, policies & procedures Build and cultivate important working relationships across field partners and internal stakeholders to ensure an enterprise approach when working with customers. Be accountable to the regional team to shape and execute on local medical strategies within planned timelines. Help to set and act on aligned clinical disease area priorities, and relay/flag any potential mismatch in priorities between internal stakeholders and the site as well as relay any key site-related decisions on behalf of the businessProvide congress and conference support, facilitating engagement between HCPs and the broader Pipeline Medical Team, as appropriate, and participating in competitive intelligence, medical booth support and related activitiesIdentify and bring insights back in house to Genentech stakeholders through efficient and effective use of CRM systems and cross functional collaboration.  Assist with Phase I - IV sponsored and supported clinical trials, health economic outcomes research, other therapeutic area specific medical collaborations; provide clinical expertise overview of performance metrics and feedback regarding  operational management of clinical trials to ensure optimal site selection and performance.   Fully understands site infrastructure and ways of working to best co-create and monitor clinical trial processes.  Supports start-up, recruitment, and retention in assigned geographies. Provides critical collaboration with CRO personnel, as appropriate, and in pre-specified mannerShare clinical and value-based expertise in the development and management of clinical and  scientific communications for customers to include publications, conference data, and educational  materials, as well as for internal Genentech communications and materials to be used in training and  development activities Ensure assigned goals, objectives, and KPIs are met and that assigned projects and other work are  completed on time, with high quality, and within budget Who you areQualifications & ExperienceAdvanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.). BSN with extensive field medical experience with a pharmaceutical companyMinimum of 5 years related work experience (clinical, managed care, or industry experience)  Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.Preferred ExperiencePrior experience as a field MSL 2 + years’ clinical research experience (either in industry or in another, related setting)2 + years' experience in therapy area strongly preferredIn-depth knowledge of clinical development programs and clinical trial managementPrior experience working in heavily matrixed organizations interfacing with clinical operations, clinical development and medical affairs organizationsLocation and Travel RequirementsBusiness travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time)This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.Applicants should reside within 30 miles of a major airport and should reside within 50 miles of the established territory. Preference will be given to applicants who reside within preferred states of residence listed above.The expected salary range for this position is $161,280 - $299,520.00.  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.BenefitsRelocation benefits are not available for this job posting.Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202602-104880Date posted : 2026-03-05Profession: Medical & Government AffairsEmployment type: Full time Read Less
  • The PositionDirector, Field Leadership & Strategic Accounts - Texoma E... Read More
    The PositionDirector, Field Leadership & Strategic Accounts - Texoma EcosystemFrom the beginning, Genentech has been a team of highly dedicated, passionate individuals. We are a place where people are united around a single purpose and an ambitious vision. Together, we aspire to deliver ever better health outcomes for patients while lowering overall healthcare costs. Our goal is to compel the customer to act on behalf of their patients while showing great commitment to the rare disease community, whose support is key.  Utilizing innovative methods to identify patients who may benefit from treatment, we must take a highly strategic approach to patient access while assisting patients and their caregivers to navigate the healthcare system.The Opportunity: Director, Field Leadership & Strategic Accounts you will be a key leader focused on delivering healthcare solutions to customers and their partners. You will work closely with the Executive Director, Healthcare Market (HED) to shape the strategic vision for the ecosystem and engage with healthcare stakeholders. You will lead a diverse team of experts to drive growth and prioritize patient outcomes, customer satisfaction, and business objectives. This includes managing an ecosystem Commercial team responsible for diverse product portfolios and aligning with ecosystem and therapeutic area priorities.You deeply understand the unique needs of each customer in their pursuit of improved patient outcomes, lower costs and improved quality of care by building, maintaining and leveraging networks and relationships in the healthcare ecosystem and co-creating solutions with customersYou contribute to and execute the strategic near and long-term vision and direction for the healthcare ecosystem set by the Executive Director, Healthcare Ecosystem and therapeutic areas to assist Squads in identifying partnerships and, under direction by the Squads executing partnerships which enhance customer experience, improve patient outcomes and deliver on business opportunities for GenentechYou lead the development and execution of customer account planning for target account(s) to deliver maximum impact opportunitiesYou are open to business travel to meet customer account needs and attend relevant therapeutic conferences.You build, lead and motivate a diverse team of people with deep functional and therapeutic area expertise. With the ecosystem leadership team, harness the collective expertise of the ecosystem team to engage effectively and compliantly across the ecosystem. Create and foster a culture that enables and requires employees at all levels to live our Operating Principles in all aspects of their work This is a field based role, it will cover Northern Texas and Oklahoma.  It is preferred that candidates live in the ecosystem for consideration.Who you are:You hold a required Bachelor’s Degree  You have 8 or more years work experience with a minimum of 3 years previous field management experience and/or marketing experience with cross-functional industry experience in commercial life sciences (pharma or biotechnology) or related industry engaging with key healthcare ecosystem players (e.g., payers, health systems).Once hired, the position title will be 'Healthcare Director' in harmony with internal roles of the same natureYour previous experience includes account management or alliance/partnership management experience, including developing and implementing account plans for various health ecosystem players (e.g., health system or hospital. You have a proven track record in coaching, training and/or mentoring peers or others as assigned; helping such others to better meet or exceed their goals, targets and other responsibilitiesYour excellent communication and interpersonal skills, including negotiation and relationship management, drive the achievement of objectives.Preferred Qualifications:You hold an advanced degree You have deep Payer Experience, ideally including local, regional and national understanding of payers in Texas & Oklahoma.You have previous Account Management Experience, ideally including local, regional and national understanding of health systems in Texas & Oklahoma.You demonstrate in-depth knowledge of strategy development, including contracting strategy, administration and pull through. You demonstrate strong executive presence and ability to engage with C-Suite executives. You have strong Account Negotiation skillsRelocation Benefits are not available for this roleThis is a field-based position.  Overnight travel may be required. This position requires significant driving of either a company provided or personal vehicle as well as prolonged periods of sitting, both of which are part of the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.The expected salary range for this position based on the primary location of Texas or Oklahoma is $209,900.00 – $389,900.00.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.BenefitsGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202604-108724Date posted : 2026-07-13Profession: Commercial, Sales & MarketingEmployment type: Full time Read Less
  • The PositionA healthier future. It’s what drives us to innovate. To co... Read More
    The PositionA healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. The OpportunityThe Metabolic dysfunction-associated steatohepatitis (MASH) Pipeline Medical Science Liaison, a part of the Cardiovascular, Renal and Metabolism (CVRM) MSL team, is a credible field medical partner responsible for providing clinical, scientific and other relevant information related to disease states and the appropriate utilization of Genentech medicines in the MASH pipeline. This field-based position will engage with healthcare providers, clinical study staff, therapeutic area experts (TAEs), population health decision makers, and patient thought leaders within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech. In collaboration with home office and regional partners, MASH Pipeline MSLs are accountable for comprehensive activities focused on delivering a successful clinical development program including, but not limited to: clinical trial recruitment focused activities, competitive intelligence, congress support, professional society engagement, and therapeutic area landscaping. In addition, MASH Pipeline MSLs may be responsible for covering multiple pipeline medicines, as well as engaging in broad clinical and scientific discussions  resulting in rich customer insights shared with key stakeholders across the organization. Preferred States of Residence• Alabama• Florida• Georgia• Mississippi• North Carolina• South Carolina• TennesseeKey ResponsibilitiesEnsure an end to end customer experience for MASH customers within the region. Demonstrate deep clinical and scientific expertise about assigned molecules/products pipeline/line of sight, franchise(s) and overall  therapeutic area(s) to exchange relevant information and insights with top tier thought leaders, clinical investigators and related staff, and healthcare decision makers within a region Build, cultivate, and leverage relationships with key external scientific and medical customers and organizations in their region(s) to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape. Develops engagement plans aligned with customer needs and preferences and global strategyEngage in continuous independent learning within the therapeutic area they represent and actively attend and participate in upskilling programs related to assigned molecules, products, disease states  and relevant business topics Respond to on and off-label questions with integrity, compliance, and adherence to legal, regulatory, and Genentech guidelines, policies & procedures Build and cultivate important working relationships across field partners and internal stakeholders to ensure an enterprise approach when working with customers. Be accountable to the regional team to shape and execute on local medical strategies within planned timelines. Help to set and act on aligned clinical disease area priorities, and relay/flag any potential mismatch in priorities between internal stakeholders and the site as well as relay any key site-related decisions on behalf of the businessProvide congress and conference support, facilitating engagement between HCPs and the broader Pipeline Medical Team, as appropriate, and participating in competitive intelligence, medical booth support and related activitiesIdentify and bring insights back in house to Genentech stakeholders through efficient and effective use of CRM systems and cross functional collaboration.  Assist with Phase I - IV sponsored and supported clinical trials, health economic outcomes research, other therapeutic area specific medical collaborations; provide clinical expertise overview of performance metrics and feedback regarding  operational management of clinical trials to ensure optimal site selection and performance.   Fully understands site infrastructure and ways of working to best co-create and monitor clinical trial processes.  Supports start-up, recruitment, and retention in assigned geographies. Provides critical collaboration with CRO personnel, as appropriate, and in pre-specified mannerShare clinical and value-based expertise in the development and management of clinical and  scientific communications for customers to include publications, conference data, and educational  materials, as well as for internal Genentech communications and materials to be used in training and  development activities Ensure assigned goals, objectives, and KPIs are met and that assigned projects and other work are  completed on time, with high quality, and within budget Who you areQualifications & ExperienceAdvanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.). BSN with extensive field medical experience with a pharmaceutical companyMinimum of 5 years related work experience (clinical, managed care, or industry experience)  Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.Preferred ExperiencePrior experience as a field MSL 2 + years’ clinical research experience (either in industry or in another, related setting)2 + years' experience in therapy area strongly preferredIn-depth knowledge of clinical development programs and clinical trial managementPrior experience working in heavily matrixed organizations interfacing with clinical operations, clinical development and medical affairs organizationsLocation and Travel RequirementsBusiness travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time)This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.Applicants should reside within 30 miles of a major airport and should reside within 50 miles of the established territory. Preference will be given to applicants who reside within preferred states of residence listed above.The expected salary range for this position is $161,280 - $299,520.00.  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.BenefitsRelocation benefits are not available for this job posting.Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202602-104880Date posted : 2026-03-05Profession: Medical & Government AffairsEmployment type: Full time Read Less
  • Senior Director - Construction Delivery  

    - San Mateo County
    The PositionWe are seeking a visionary Senior Director of Construction... Read More
    The PositionWe are seeking a visionary Senior Director of Construction Delivery to lead one of Genentech's most significant capital initiatives—a billion-dollar-plus CAPEX project at our South San Francisco campus. This pivotal leadership role offers the unique opportunity to shape the strategic vision and execution of a large-scale, complex construction program while driving transformative change across our capital project delivery capabilities. You will command a diverse, integrated team of senior project managers, engineers, and functional leads, overseeing every phase of project lifecycle from inception through completion. Your strategic oversight, exceptional leadership, and unwavering commitment to safety, quality, and compliance will be instrumental in delivering world-class results that align with our Campus vision and advance Genentech's global operations. If you're a proven construction leader with deep expertise in managing complex, large-scale projects, a passion for building high-performing teams, and a drive to champion innovation and continuous improvement, we invite you to apply.The OpportunityDrive strategic construction oversight for significant capital investments in alignment with the Campus vision plan. Provide strategic construction leadership to a diverse team of architects, contractors, consultants, project managers, and general contractors.Cultivate a collaborative and high-performance team environment for seamless project execution and delivery, leveraging internal and external resources effectively.Oversee the entire lifecycle of large-scale construction projects, ensuring alignment with strategic goals from inception through to completion.Ensure timely, cost-effective, and quality delivery of projects while meeting financial targets and strategic objectives.Guarantee compliance with local, state, and federal regulations and maintain rigorous standards in all aspects of project delivery.Strategically engage with government bodies to secure necessary permits and approvals for project advancement.Safety, Quality, and Compliance: Champion a world-class safety culture for the entire project. Ensure the project adheres to all Genentech engineering standards, and regulatory compliance from design through final validation.Supplier & Contract Management: Lead the selection and strategic management of construction managers, general contractors and other key suppliers capable of executing a project of this scale. Personally manage the relationships with the senior leadership of these partner firms to ensure performance and alignment.Organizational Improvement: Drive continuous improvement initiatives not only for the project but also to advance the capital project delivery capabilities within the broader CVP and CD organization.Team Development & Leadership: This role will hire, develop, and lead a large, integrated project team composed of senior project managers, engineers, and functional leads. The leader is responsible for fostering a culture of collaboration, accountability, and excellence by providing direction and coaching on how best to execute the work, helping to resolve escalated issues, and guiding senior staff in their career development.Spearhead the bidding and negotiation processes, expertly managing contracts with contractors, consultants, and other critical stakeholders.Develop, manage, and strategically allocate financial resources, ensuring rigorous budgeting, forecasting, and cost control across projects.Foster financial accountability and transparency throughout the project lifecycle.Proactively identify, assess, and mitigate risks, employing strategic risk management and insurance minimization approaches.Establish and maintain robust communication channels to keep all stakeholders informed and aligned.Continuously evaluate and refine project delivery processes to enhance efficiency and effectiveness.Stay abreast of industry trends, championing best practices and integrating emerging technologies into project delivery strategies.Ensure adherence to Roche directives, local building codes, fire protection regulations, procurement guidelines, and technical standards.Define and implement strategic frameworks for planning, procurement, execution, commissioning, and financial resource coordination.Foster cross-functional collaboration with global stakeholders, including colleagues in the SET network, to leverage lessons learned and best practices.Integrate innovative and sustainable solutions into projects, advocating for advanced processes, technologies, and methodologies within Genentech and Roche.Who You AreEducation and Expertise:Bachelor’s degree in Architecture, Engineering (Civil, Structural, Chemical, Mechanical, Electrical), Quality Surveying or Construction Management.10+ years of extensive experience in managing large-scale construction projects, with expertise in Project Management in California.Proven track record in delivering large ($500M+), complex projects within large existing campus environments.Relocation benefits are not available for this posting.The expected salary range for this position based on the primary location of California is $201,500 - $374,100.  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.Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202604-109330Date posted : 2026-06-15Profession: Research & DevelopmentEmployment type: Full time Read Less
  • Senior Thought Leader Liaison - Neuroimmunology  

    - Clark County
    The PositionSenior Thought Leader Liaison (TLL) - Neuroimmunology​​​​​... Read More
    The PositionSenior Thought Leader Liaison (TLL) - Neuroimmunology​​​​​​​We’re passionate about delivering on Our Promise to improve the lives of patients and create healthier communities for all. We foster a culture of inclusivity, integrity and creativity while boldly pursuing answers to the world’s most complex health challenges and transforming society.The Opportunity:The Senior TLL role at Genentech acts as the lead Commercial enterprise bridge to National & Regional Therapeutic Area Experts (TAEs) across Therapeutic Areas (TAs), operating as a proactive strategic partner who shapes markets and converts TAE influence into measurable results. The Senior TLL enables demand and patient access by serving as the trusted connection to priority TAEs, converting credibility into enterprise impact, translating scientific insights into commercial execution, and shaping TA narratives that drive belief, standard of care, and competitive positioning. The Senior TLL will demonstrate capabilities to translate TAE insights into actionable feedback to shape brand and squad strategies and execution. The role translates squad priorities into regional Customer Engagement (CE) opportunities and serves as the coordinated interface between external TAE engagement and internal strategy. TLLs operate with agility, adapting focus to evolving enterprise and portfolio priorities.  Success in this role is demonstrated by accelerated speed to peak for priority launches, decision-shaping TAE engagement, and clear impact on therapeutic area and brand strategy based on outcome-based KPIs.Key Roles & Responsibilities:Establish and foster effective partnerships with TAEs Enable demand and patient access by influencing TAE perception and advocacy of products through clinical data education, mapping their influence, and mobilizing TAEs as advocates to accelerate product adoption and account readiness.Enable appropriate demand by building trust and accelerating informed decision-making with TAEs across the lifecycle (pre- and post-launch). Rapidly translate bi-directional insights into execution by synthesizing TAE feedback, competitive intelligence, and market dynamics to shape TA/brand strategy, collaborating with Marketing, Medical, Global and CE partners Actively participate in core Marketing and TLL sub-teams (e.g., ad boards, insights, congresses) and lead cross-functional alignment across Marketing, Medical, CE, Compliance, Legal, and Global teams to focus TLL efforts on key TA and launch needs.Proactively shape TAE understanding by providing timely clinical data and competitive context, ensuring misperceptions are connected compliantly to enable informed advocacy and faster patient access.Act with urgency to ensure TAEs have current clinical data and competitive context, compliantly address misperceptions in real-time, and enable informed TAE advocacy to accelerate patient accessMaintain end-to-end accountability for TAEs in assigned scope, from pre-launch identification and engagement strategy through market shaping, advocacy development, and sustained partnership Partner with Medical to co-lead overarching TAE strategy for brands, indications, and launches, with TLL owning demand enablement and Commercial engagement strategy while Medical owns scientific exchange; collaborate to ensure complementary execution with clear role boundaries Compliantly manage Fee-for-service activities that include TAEs (selection/pull through as appropriate)Demonstrate agility by prioritizing engagement based on enterprise criteria (launch stage, TAE influence, barrier intensity, tier designation) to maximize impact and accelerate speed to peak. Works autonomously to make decisions and act, in close alignment with the full product value proposition, customer positioning, and Squad prioritiesDrive KPIs tied to speed to peak percentage of market, quality & depth of TAE engagement, and strategic influence on TA & brand decisions.Accountable for being fully knowledgeable of and compliant with all relevant company policies and procedures, and applicable laws and regulations that govern the conduct of GNE activities Face-to-face customer engagement is required to maximize customer impact, requiring travel within the territory as neededThis is a field based position and the ideal candidate can live anywhere in the following states: Nevada, Utah, North Dakota, Minnesota, South Dakota, Nebraska, Iowa, Idaho, Montana, Wyoming, Eastern Washington or Oregon. Proximity to a major airport is preferred due to travel requirements.  Relocation benefits are not provided for this role. Senior Thought Leader Liaisons are expected to consistently perform at a proficient level (proficient is defined as leveraging competencies across the business in a consistent, integrated way)Customer Understanding- I’m always learning about my customers, what they need, and the world they live in.Competitive Value Creation - I determine the relevant, competitive, and profitable value story we offer to customers.Strategy Development - I make smart choices about what efforts will help achieve customers’ goals and our goals.Execution Readiness - I rally the organization to plan, coordinate, and pull through the strategy together.Delivery & Optimization Across Channels - I make sure our story is reaching customers in a seamless, memorable experience.Measurement & Iteration - I evaluate everything we do, and adjust, stop, or start for continuous improvement.Knowledge/Skills:Market & Customer Expertise Deep knowledge of National and Regional TAEs with a preference for strong relationships among TAEs within geographyDeep knowledge of each customer type (e.g. HCPs, patients, payers, IDNs, distributors, pathways) and how TAEs may engage with various customer typesAbility to educate and challenge TAEsStrategic & Enterprise Orientation Understanding of partners, their roles and leveraging their expertise to effectively partner, engage, and mobilize key internal stakeholders. Ability to articulate business problems and identify solutions Ability to translate enterprise and portfolio strategy into tactical TAE engagement plans that align regional execution with brand priorities and TA goals Ability to successfully manage cross-functional projects in collaboration with other internal stakeholders and vendors Ability to influence and inspire individuals and teams across the CMG network, from front-line employees to the executive levelComfort operating in an outcomes-based performance environment Insight Translation & Analytic Ability  Advanced ability to interpret and synthesize quantitative and qualitative data across market dynamics, customer sentiment, competitive intelligence, and TAE advocacy trends, translating insights into strategic recommendations and outcome-based metrics that demonstrate measurable enterprise impact Ability to utilize everyday AI, computer programs to build and share presentations, utilize spreadsheets to decipher important insights, and host virtual meetings with internal and external stakeholders/customersAgility & TA Mobility Ability to rapidly ramp up new or highly competitive therapeutic areas while thoughtfully building credibility and new relationshipsStrong prioritization skills to balance maintaining high-value relationships with supporting emerging launch or enterprise needs.Ability to flex and thrive in an ambiguous environment undergoing transformational changeAbility to develop and leverage TAE influence maps at national, regional, and local levels to identify broader networks, optimize engagement strategies, and mobilize TAEs as catalysts for accelerating product adoptionNon-Clinical & Performance Marketing Fluency Demonstrated ability to integrate clinical acumen with non-clinical levers (market access, reimbursement, competitive dynamics) and performance marketing fluency to enable comprehensive TAE engagement and demand enablementWho You Are:Bachelors’ Degree A minimum of 5 years cross-functional industry experience in life sciences (pharma or biotechnology) or related industry (e.g., payers, health systems), is requiredAdditional Desired Candidate Qualifications & Experience:Graduate Level degreeNeuroImmunology and/or MS experience Thought Leader Liaison experience with demonstrated ability to adapt across multiple TAs, product lifecycle stages, and shifting enterprise priorities based on market dynamics and launch opportunities. Previous experience in Commercial or Sales functions Experience in shaping or influencing marketing strategies, plans, and tactics Proven and thorough knowledge of Commercial issues associated with highly competitive therapeutic area Proven track record of consistent achievement or overachievement in assigned responsibilities, goals, objectives and any other relevant metricsPrevious experience building, implementing and seamlessly executing action plans, programs and related activitiesLocation:Relocation benefits are not provided for this role. Individual must reside within the territory boundaries given extensive travel requirements of the TLL roleBusiness travel, by air or car, is regularly required up to 60%This position requires significant business travel. Traveling by air or by car is regularly required as well as prolonged periods of sitting, both of which are part of the essential duties and responsibilities of the position. As a result, Genentech, Inc. (Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.The expected salary range for this position is $162,500 - $301,700.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  This position is eligible to earn incentive compensation that is calculated and paid in accordance with the applicable Incentive Compensation Plan for the role. This position also qualifies for the benefits detailed at the link provided below.BenefitsRoche Operating PrinciplesPut Patients First: I always act as if patients I know are in the room and do what’s best for themFollow the science: I seek answers through experiments, data and debate, and act on factsAct as one team: I care, collaborate and commit without boundaries, and trust others to do their partEmbrace differences: I seek diverse perspectives, invite opposing views, and challenge myself and othersAccelerate learning: I push to learn new things even if difficult, and openly share my successes and failuresSimplify radically: I eliminate complexity, reuse with pride, and accomplish more with lessMake impact now: I take accountability to do what’s right, deliver value fast, and don’t wait for certaintyThink long term: I choose actions today that benefit future generationsGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202605-111514Date posted : 2026-07-10Profession: Commercial, Sales & MarketingEmployment type: Full time Read Less
  • The PositionGreat medicine can't change the world if it never leaves t... Read More
    The PositionGreat medicine can't change the world if it never leaves the lab. Our Pharma Technical Operations (PT) organization is the global backbone that transforms scientific discoveries into real-world therapies. Joining our Global Legal Technical Operations & Facilities team means stepping onto a highly collaborative, global team of experts. Together, we provide the proactive legal support that empowers PT to manufacture and deliver medicines safely and efficiently. You’ll be trusted to advise on complex, high-stakes matters, knowing that your daily work supports our patients and our company’s global ambition to prevent, stop and cure diseases. We are seeking to hire a Corporate Counsel in Global Legal Technical Operations & Facilities. This team member will focus on global support to PT and its sites involving regulatory and transactional counseling on environmental, health & safety matters, FDA/cGMP, manufacturing supply and development agreements, and other related matters.The OpportunityKey responsibilities of this individual contributor role may include but not be limited to the following:Providing legal advice and strategic counseling to PT sites, Environmental Health and Safety (EHS) departments, global EHS functions, and other business units.Advising and representing our manufacturing sites on EHS compliance and enforcement matters, sustainability, and environmental land use issues.Coordinating environmental due diligence; drafting and negotiating EHS and related provisions of contracts; and counseling on environmental site remediation.Advising on regulatory and compliance matters arising under the Federal Food, Drug, and Cosmetic Act related to manufacturing practices (cGMP), quality system requirements, and other issues and agreements involving quality considerations. Preparing and negotiating manufacturing supply and development agreements, and advising on related transactional issues key to manufacturing operations.Managing outside counsel retained to support legal matters.The HowLegal excellence accelerates in combination with the right business- and solutions-focused attitude, mindset, and ways of working. Here is who we are looking for:Communication and LeadershipPro-active and confident individual who is committed to driving change.Strong verbal and written communication skills.Ability to communicate complex and highly technical information clearly and concisely.Commitment to working as a team player in a multinational legal department.Excellent interpersonal skills with high cross-cultural sensitivity.Willingness to travel.Our ExpectationsStrong business acumen; sensitive to business needs; views change as an opportunity; eager to work in a fast paced environment.Best in class attitude; challenges status quo constructively and contributes to improvements; results oriented; ability to influence; solutions oriented mindset.Who You Are5+ years of EHS or manufacturing related legal experience, ideally in a pharma/biotech corporate setting and/or in a law firm or relevant government agency.A U.S. law degree (J.D.) and current “good standing” admission to at least one U.S. state bar, or be eligible to apply to California’s Registered In-House Counsel program.Demonstrated experience and track record of success or committed interest in:Providing EHS regulatory compliance advice to industrial clients, preferably to the pharmaceutical or biotech industries;Providing manufacturing support in pharmaceutical or biotech industries, such as regulatory counseling on FDA/cGMP related matters.LocationThis role is located at Genentech’s South San Francisco, California campus. A remote working arrangement is not available.Relocation benefits are not available for this position. The expected salary range for this position based on the primary location of California is $181,800 to $337,600. 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.BenefitsGenentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202606-116629Date posted : 2026-06-29Profession: Business Strategy & DeliveryEmployment type: Full time Read Less
  • Global Data Acquisition Lead  

    - San Mateo County
    The PositionWho We areRoche - we advance science so that we all have m... Read More
    The PositionWho We areRoche - we advance science so that we all have more time with the people we love.The Advanced Analytics for Business Insights (AABI) team, part of the Portfolio Strategy & Insights function, is dedicated to solving complex healthcare challenges and improving patient outcomes. AABI enables our business partners across Global Pharma Strategy (GPS), Medical Affairs (PDMA), Pharma International (PI)and other functions to make impactful decisions by leveraging data, analytics, and AI to enable fast, targeted actions in rapidly evolving business contexts.In AABI, you will work as a trusted advisor and expert, recommending critical decisions and actions to be taken with credibility and a focus on driving measurable impact. You will be part of a diverse, inclusive team that reflects the world we serve, thriving in a welcoming culture built on collaboration and innovation.This role will report to the Head of Data Asset Management.The PositionAs the Global Data Acquisition Lead, you will be leading all data acquisitions across GTM, while also serving as the catalyst for innovation, with out-of-the-box thinking and external partnerships. This role will lead the global commercial data office (GCDO) responsible for driving the data strategy, assess market landscape, evaluate data vendors and source data assets that drive key business outcomes in support of One Pharma Strategy. You will act as a catalyst to enable the AI data ecosystem to drive key initiatives and global AI data products.The lead will operate with an enterprise mindset and work closely with Global Procurement (GP), Finance, Roche Digital Technology (RDT) to enable the platforms and solutions; Global Privacy Office (GPO) to drive compliance policies; key data vendors and partners across the globe to drive acquisition and operations.Key Responsibilities:  Run the Global Commercial Data Office to enable all commercial data acquisition across global and 80+ affiliates, governed through a centralized model, in partnership with the procurement and finance teamsPartner with stakeholders across GPS, PI, PD, PDMA, affiliates and Roche other divisions, serving as their data stewards/experts to drive fit-for-purpose data acquisition, training, adoption, monitoring usage/value and decommissioningEstablish data as an enterprise asset by x-functional partnering & serving as the data steward / expert across the enterpriseLead major data acquisition contracts in partnership with procurementWork in sync with data governance to enable seamless integration of data purchases in the data catalog.Collaborate cross-functionally to design, build and operate an enterprise data marketplace, for easy access to information about data assetsServe as the in-house expert of the existing and evolving data assets in the industryWork closely with peers and senior leaders in - ecosystem insights, CI, global access, therapeutic area teams; affiliate leadership/data & insights champions; Genentech data office team - to develop and implement a harmonized data acquisition process, data on-boarding, and utilization considerationsEngage with data vendors to evaluate their products and offerings in alignment to our business, drive data contracts and enable cost effective enterprise/above-country data procurement strategy, where possible, to maximize the value of dataServe as the internal expert for consulting on the existing data sources, along with the pros and cons of the different assets Organize knowledge sharing sessions, bringing in industry experts and vendor partners with information on trends and best practicesCollaborate with data consumers as the data expert to help deliver actionable insights to the businessAccountable for resource allocation and investments both in the near-term and long-term; work with affiliate leads and finance teams to make resourcing tradeoff decisionsOperate with enterprise mindset, with a strong focus on outcome  Qualifications:Bachelor's degree with 10+ years’ experience with extensive knowledge of pharma data and technology; or 6+ years with MBA/MS with extensive knowledge of pharma data and technologyStrong understanding of the pharmaceutical data domain, both global and especially regional & country level ecosystem.Knowledge of commercial operations and analytics approaches in biopharma including descriptive and predictive analyticsUnderstanding of emerging capabilities in natural language processing, unstructured data, etc. and potential application in pharma/health careAbility to help translate complex data insights into actionable business recommendationsExcellent influencing and networking skills paired with stakeholder management experience in a multi-layered global environmentExcellent communication and stakeholder management skills, with demonstrated success in facilitating cross-functional collaboration.Experience with Cloud platforms (like AWS) preferredExperience in Agile methodology and execution and design thinking Availability to travel internationally as required     Location:This position can be based in South San Francisco or Basel and relocation benefits are not available.The expected salary range for this position based on the primary location of South San Francisco, CA is $160,900 - $298,900 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.Benefits#LI-NN1Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.Job SummaryJob number: 202607-118298Date posted : 2026-07-17Profession: Data Science & AI / MLEmployment type: Full time Read Less

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