Full-Time

Head – Innovation Accelerator Data Science

Genentech

Genentech

10,001+ employees

Biotech firm creating medicines via R&D

Compensation Overview

$254.4k - $472.4k/yr

+ Bonus

Boston, MA, USA + 1 more

More locations: San Bruno, CA, USA

In Person

Category
Data & Analytics (1)
Required Skills
Scikit-learn
Agile
Python
Data Science
Tensorflow
R
Pytorch
Xgboost
DevOps
Requirements
  • An advanced degree (Master’s or PhD) in Computer Science, Data Science, Statistics, Engineering, or a related technical field
  • 15+ years of hands-on experience in software engineering, data science, or technical innovation, ideally within research and development or regulated environments
  • 4+ years in a leadership role managing multidisciplinary technical teams
  • Proven experience driving technology delivery from prototyping to scaled implementation
  • Deep expertise in modern data and software development technologies and architectural practices
  • Proficient with Python or R, and machine learning libraries such as scikit-learn, XGBoost, TensorFlow, or PyTorch
  • Strong understanding of supervised and unsupervised learning, statistical modeling, and experimental design
  • Familiar with software development practices including version control, testing, and collaborative coding
  • Experience running simulations or analyses in a high-performing computing environment
  • Knowledge of four or more of the following: epidemiology including causal inference for observational real-world data or real-world evidence; Bayesian statistics; decision theory including multiple criteria decision analysis, utility elicitation, decision simulation models, or value of information; clinical outcomes research using data from electronic health records; discovery mechanisms and evidence generation pathways for novel biomarkers and risk scores; interpretable machine learning; methods to incorporate knowledge graphs, ontologies, or other forms of structured information; probabilistic programming languages; complex or innovative clinical trial designs including adaptive stopping, seamless Phase 2/Phase 3 designs
  • Strong track record in managing resources, planning capacity, and balancing competing priorities
  • Excellent communication and stakeholder management skills
  • Fluent in agile delivery, DevOps, or other modern ways of working
  • Passion for continuous learning
  • Passion for mentoring colleagues of all backgrounds
  • Capacity for independent thinking and ability to make decisions based upon sound principles
  • Excellent strategic agility including problem-solving and critical thinking, with agility beyond the technical domain
  • Respect for cultural differences in the global workplace
  • Excellent verbal and written communication skills with the ability to explain complex technical concepts clearly
Responsibilities
  • Provide technical leadership across early exploration and productization phases of innovation projects, ensuring alignment with departmental goals and enterprise direction
  • Act as subject matter expert and single point of escalation/problem resolution for applied data science and software engineering within the innovation portfolio
  • Influence PDD data, design and data science (three-dimensional) strategy and in-silico strategy and roadmaps through strategic technical leadership/expertise
  • Make architectural decisions independently and ensure adherence to best practices for scalability, performance, reliability, and compliance
  • Oversee execution quality, technical risk management, and project velocity across multiple high-impact workstreams and domains
  • Establish and enforce technical standards, enabling reuse, modularity, and robust design across solution development
  • Lead technical capacity planning and resource deployment within the team, prioritizing based on departmental strategy and portfolio needs
  • Collaborate with cross-functional and enterprise partners to translate innovation opportunities into feasible, impactful, and technically sound solutions
  • Drive the Innovation Accelerator portfolio through contribution to governance, resource planning, and progress reviews
  • Identify and integrate new technologies and platforms, applying functional expertise and organizational context to maximize department performance
  • Ensure traceability, reproducibility, and risk mitigation through robust documentation and engineering practices across all technical deliveries
  • Manage a multidisciplinary team of specialists and junior leaders (e.g., data scientists, software engineers), ensuring accountability for delivery, performance, and development
  • Oversee hiring, onboarding, workforce planning, and succession management aligned to departmental capabilities and strategic growth areas
  • Coach and mentor team members to enhance their individual performance and long-term potential, developing future technical leaders across roles and backgrounds
  • Foster a high-performance, inclusive culture focused on collaboration, ownership, and continuous improvement
  • Set development goals, conduct performance evaluations, and guide career progression based on business priorities and professional aspirations
  • Manage team deployment and resource allocation across a complex portfolio of innovation projects, balancing individual growth with business needs
  • Execute short-term department plans by managing priorities, budget, and capacity in coordination with function leadership
  • Influence senior stakeholders and functional leadership to secure alignment, resources, and sponsorship for technical priorities
Desired Qualifications
  • Experience in pharma, life sciences, or healthtech sectors
  • Familiarity with regulated environments and compliance-driven product development
  • Exposure to innovation frameworks (lean startup, dual-track agile)
  • Demonstrated ability to assess and integrate emerging technologies (e.g., GenAI, ML Ops, cloud platforms)

Genentech is a biotechnology company focused on researching and developing medicines and therapies to address unmet medical needs. It uses large-scale R&D, with about 13,500 employees and 40 approved medicines; it develops biologics and other therapies marketed through healthcare providers, generating revenue from sales. It differentiates itself with a large patent portfolio (around 20,000 patents) and multiple FDA Breakthrough Therapy Designations, along with a patient-centric approach that weighs access and affordability. Its goal is to advance medical science and deliver high-quality, effective therapies that improve patient health and support the broader medical community.

Company Size

10,001+

Company Stage

Grant

Total Funding

$48.8B

Headquarters

San Francisco, California

Founded

1976

Simplify Jobs

Simplify's Take

What believers are saying

  • FDA approved Vabysmo expanded label for RVO beyond six months in 2026.
  • $450 million Oceanside facility boosts production by 2026.
  • ARVO 2026 VOYAGER study shows Vabysmo retinal drying in six months.

What critics are saying

  • Regeneron Eylea HD erodes Vabysmo share in DME by 2026.
  • Mylan Formycon Lucentis biosimilars slash sales mid-2026.
  • Flizasertib phase 2 failure terminated program in Q1 2026.

What makes Genentech unique

  • Genentech founded biotech industry in 1976 with synthetic human insulin.
  • Vabysmo bispecific antibody targets Ang-2 and VEGF-A for ophthalmology.
  • Holds 20,000 patents and 39 FDA Breakthrough Therapy Designations.

Help us improve and share your feedback! Did you find this helpful?

Your Connections

People at Genentech who can refer or advise you

Benefits

Performance Bonus

Relocation Assistance

Company News

Yahoo Finance
Apr 13th, 2026
BRAF-mutated NSCLC market set to grow with emerging therapies from Novartis, Genentech targeting 10,000 US cases

A new market report projects growth in BRAF-mutated non-small cell lung cancer treatments through 2036 across the US, EU5 and Japan. The United States recorded nearly 201,200 NSCLC cases in 2022, with approximately 10,000 involving BRAF mutations, expected to increase substantially by 2034. Currently, only Novartis's Tafinlar and Mekinist combination therapy is approved for this mutation, having gained approval in 2017. The BRAF-mutated NSCLC market generated around $250 million in EU4 and UK markets in 2022. Emerging therapies in development include Plixorafenib and CFT1946, which target various BRAF mutations. The report identifies significant unmet medical needs and opportunities for new treatments, with market expansion anticipated through 2036 as new products enter clinical development.

Eyewire
Apr 10th, 2026
Genentech secures FDA approval for extended use of Vabysmo in retinal vein occlusion.

Genentech secures FDA approval for extended use of Vabysmo in retinal vein occlusion. Key Takeaways * The FDA approved an expanded label for Vabysmo, allowing treatment of macular edema due to retinal vein occlusion (RVO) beyond 6 months. * The update aims to enables greater treatment continuity, helping reduce the need for therapy switches * The revised dosing guidance offers more flexibility to tailor care and align treatment with real-world practice, potentially improving long-term patient outcomes Genentech announced that the FDA has approved an updated label for Vabysmo (faricimab-svoa), allowing its use in the treatment of macular edema due to retinal vein occlusion (RVO) beyond 6 months. The newly approved label expansion enables longer-term treatment continuity for patients who are already using Vabysmo. "This label update reinforces our commitment to delivering consistent, long-term solutions for patients with vision impairment," said Levi Garraway, MD, PhD, chief medical officer and head of Global Product Development at Genentech. "With Vabysmo's well-established efficacy, this label update should help minimize disruptive treatment switches in patients with RVO who are benefitting from Vabysmo." Vabysmo is the first bispecific antibody approved for ophthalmic use. It works by targeting and inhibiting two key signaling pathways associated with vision-threatening retinal conditions: angiopoietin-2 (Ang-2) and vascular endothelial growth factor-A (VEGF-A).

PR Newswire
Mar 25th, 2026
Lupus Foundation of America announces Genentech as national presenting sponsor of Walk to End Lupus Now(R).

Lupus Foundation of America announces Genentech as national presenting sponsor of Walk to End Lupus Now(R). Mar 25, 2026, 10:00 ET This national partnership strengthens efforts to fund lupus research, education, and support programs nationwide. WASHINGTON, March 25, 2026 /PRNewswire/ - The Lupus Foundation of America proudly announced that Genentech, a member of the Roche Group, will serve as this year's presenting sponsor of the Walk to End Lupus Now(R), the nation's largest lupus awareness and fundraising program taking place in 30 communities across the United States. Lupus is a chronic autoimmune disease that affects millions of people worldwide, including 1.5 million in the U.S. Symptoms can range from severe fatigue and brain fog to life-threatening complications and organ damage. While lupus can affect anyone, nine out of ten people with lupus are women, and it disproportionately impacts Black/African American, Hispanic/Latino, Native American, and Asian/Pacific Islander populations. Walk to End Lupus Now(R) brings people living with lupus and their caregivers, families, and supporters together to raise critical funds for lupus research, education, advocacy, and support programs. Through this partnership, Genentech will help the Lupus Foundation of America further drive progress in lupus care, expand essential resources, and bring us closer to a world without lupus. "We are incredibly grateful to Genentech for stepping forward as the presenting sponsor of the 2026 Walk to End Lupus Now initiative," said Louise Vetter, President and CEO of the Lupus Foundation of America. "Genentech's commitment to the lupus community reflects a shared dedication to improving the lives of the millions of people affected by this complex and unpredictable disease. Together, we are advancing the quality of care for lupus families and ensuring that future generations have access to safe and effective treatments for this debilitating, chronic disease." "Genentech has spent the last three decades pursuing scientific breakthroughs for patients living with lupus," said Girish Mulye, Vice President and Head of Genentech Immunology. "Serving as presenting sponsor for the Lupus Foundation of America's Walk to End Lupus Now affirms our commitment to partnering with the lupus community in the fight for improved care. We walk for awareness and to turn scientific potential into impact for every person affected by this disease." Everyone can join the Walk to End Lupus Now program by rallying friends and family, organizing a team, engaging their social networks, raising critical funds, and fostering awareness to advance the Lupus Foundation of America's mission to end lupus. About the Lupus Foundation of America The Lupus Foundation of America is the premier patient advocacy organization devoted to solving the mystery of lupus, a devastating autoimmune condition where the immune system attacks organs throughout the body, while giving caring support to those who suffer from its brutal impact. Through a comprehensive program of research, education, and advocacy, we lead the fight to improve the quality of life for all people affected by lupus. Learn more about the Lupus Foundation of America at lupus.org. About Lupus Lupus is an unpredictable and complex autoimmune disease that can affect multiple parts of the body. It is difficult to diagnose, challenging to treat, and often misunderstood. Lupus can cause symptoms ranging from skin rashes to organ damage and can be life-threatening. Despite its devastating impact, research on lupus remains underfunded relative to the disease's scope. SOURCE Lupus Foundation of America, Inc.

Fierce Biotech
Mar 19th, 2026
Genentech shreds RIPK1 inhibitor from pipeline after early ph. 2 failure.

Genentech shreds RIPK1 inhibitor from pipeline after early ph. 2 failure. Genentech has elected to stop a phase 2 trial of a RIPK1 inhibitor early and dump the asset after an analysis revealed the candidate was unlikely to meet the study's primary endpoint. Flizasertib, also known as GDC-8264, was removed from Genentech's pipeline in the first quarter of this year, a company spokesperson confirmed to Fierce Biotech, after interim data "indicated that the study was unlikely to demonstrate a significant clinical benefit." The Roche subsidiary was testing flizasertib's ability to treat acute kidney injury after heart surgery, a common complication that can follow procedures like coronary artery bypass, valve replacements and aortic surgeries due to reduced blood flow to the filtering organs. The terminated study was a randomized, placebo-controlled phase 2 trial that began in January 2025 and enrolled 67 patients, according to the federal clinical trials database. The primary efficacy endpoint, which flizasertib was not set to deliver on, was the percentage of patients who develop persistent complications in the 90 days following a surgery-induced kidney injury. Genentech announced the discovery of GDC-8264 last fall in a paper (PDF) published in the Journal of Medicinal Chemistry. At the time, the biotech's scientists described the small molecule as having "excellent target selectivity and druglike attributes for once-daily oral dosing." Flizasertib's descent is another blow for the RIPK1 inhibitor field, which has struggled to produce an approved medicine despite numerous biotechs and Big Pharmas pursuing the target. RIPK stands for receptor-interacting serine/threonine-protein kinase, with RIPK1 part of a family of enzymes that help regulate inflammation and cell death. GSK had the first-ever RIPK1 inhibitor okayed for clinical research back in 2014, but later kicked it back to the research stage; that asset, GSK2982772, is no longer listed in GSK's pipeline. The British pharma also dropped a different candidate in the class for the development of prostate cancer in 2019. French drugmaker Sanofi bought into the modality in 2018 through a pact with Denali Therapeutics, but has steadily pulled back due to a string of phase 2 failures. Sanofi scrapped its last remaining Denali RIPK1 inhibitor at the end of January. Eli Lilly, too, has had a rethink of RIPK1. After signing a deal worth as much as $960 million with Rigel Pharmaceuticals back in 2021, Lilly reneged on the central nervous system-focused portion of the partnership. The star of that deal, though, Rigel's ocadusertib (now coded LY3871801), is still being tested in a phase 2 trial for rheumatoid arthritis. Meanwhile, there may be potential for an already approved drug to be repurposed as a RIPK1 inhibitor. Last summer, a team of Korean scientists discovered that phensuximide, which was once used to treat epilepsy, can restrain RIPK1's inflammatory activity. Let Google know we are your trusted source. Add our editorial as a preferred source in your search results.

North Carolina Biotechnology Center
Mar 10th, 2026
Automation, partnerships driving advances in NC pharma manufacturing.

Automation, partnerships driving advances in NC pharma manufacturing. With roughly 35,000 people employed in life sciences manufacturing, North Carolina has emerged as one of the leading destinations for biopharma companies building or expanding their operations. It's no surprise, then, that the state's biopharma manufacturers are investing heavily in technology, partnerships and people to maintain their competitive edge. That focus was front and center during the recent collaboration with INTERPHEX, the North Carolina Biotechnology Center and FUJIFILM Biotechnologies. "I'm excited about the impact we're having in North Carolina and what we're doing here to establish ourselves as the area to compete with in the U.S.," said Laurie Braxton, senior vice president and site leader of North Carolina operations for FUJIFILM Biotechnologies. "We're not just giving people jobs for a few days or a few years. We're creating career paths that are going to allow people to excel in something that they're passionate about." Braxton was speaking at a recent daylong event on North Carolina life sciences manufacturing called "INTERPHEX On the Ground - North Carolina: The Inaugural Immersive Experience for Pharma and Biotech Professionals." The experience was organized by INTERPHEX, a pharma and biotech event held annually in New York City (April 21-23, 2026). INTERPHEX On the Ground was co-hosted by FUJIFILM Biotechnologies, a leading global contract development and manufacturing organization and NCBiotech. The day included panel discussions and networking opportunities at NCBiotech's Research Triangle Park conference center and a panel and facility tour at FUJIFILM Biotechnologies' new cell culture manufacturing facility in Holly Springs. Technology assisting, not replacing people. Life sciences leaders provided insights into the ways their companies are building smarter, more advanced manufacturing capabilities. Advances in automation and artificial intelligence are helping manufacturers speed production of medicines while reducing error rates and downtime. While AI plays a key role, it doesn't work without people and processes, Matt Foster, Research Triangle Park site head at Eli Lilly, said during a panel discussion on the role of automation in therapeutic innovation. "I think AI is in combination with HI - human intelligence - in a partnership, not just an outsource," he said. "You have got to understand principles first to trust the AI tool or application that's going to benefit you and make you better." One application of AI that's improving drug manufacturing is the use of digital twins to simulate production processes and facilities. Joash Mudalige, vice president and site head for Genentech's 700,000-square-foot manufacturing facility under construction in Holly Springs, said the company is using digital twins to design facilities with a high degree of precision. "We have the entire model of the plant built on a digital twin, down to the varying temperature in the warehouse," he said. "What you can do through a tool like a digital twin, going into the design phase now, is just incredible." Collaboration over competition. The role of partnerships in biopharma manufacturing also took center stage during the day. Developing relationships across the industry is especially critical for contract development and manufacturing organizations (CDMOs) such as FUJIFILM Biotechnologies, which provides drug development and manufacturing services to pharmaceutical companies. FUJIFILM Biotechnologies' Braxton said the growing presence of manufacturing facilities in North Carolina is contributing to an environment marked more by collaboration than competition. "What we've had a lot of conversations about is, how do we not compete against each other, but how do we actually learn from each other, and how do we spread and share the wealth?" she said. One way to foster collaboration, several speakers said, is to join forces in support of education and training programs through the state's universities, community colleges and corporate training centers. Mevluet Yilmaz, director of sales for Optima Pharma, a German-owned company with a pharmaceutical filling and packaging operation in Knightdale, said workforce training is an area requiring significant investment on the part of pharma manufacturers. "Having trained operators that can operate the equipment is really key," he said. "Having a solid training program can really help them to understand and feel comfortable touching the equipment." Kyle Marshall, NCBiotech Writer Tue, 03/10/2026 Related life sciences news. March 17, 2026 The tenth edition of Triad BioNight, a celebration of bioscience growth and recognition of industry leaders in North Carolina's Piedmont Triad region, is expected to attract over 400 attendees in May. This long-standing, iconic event, hosted by the North Carolina Biotechnology Center and its Piedmont Triad Regional Advisory Committee, is scheduled for Wednesday, May 27, from 6:00 to 9:00 p.m., at the Grandover Resort in Greensboro. March 12, 2026 Coriolis Pharma, a global contract research and development organization, celebrated the grand opening of its new North America headquarters and laboratory, marking the start of operations at the Alexandria Center for Advanced Technologies (ACAT) in North Carolina's Research Triangle Park (RTP). March 9, 2026 As North Carolina's life sciences sector continues to grow, women are playing a central role in shaping its future. Across startups, pharmaceutical companies and economic development organizations, women launch companies, lead the manufacturing of new medicines and attract new companies to North Carolina - shaping North Carolina's life sciences ecosystem at every level.