Principal ADS Program Lead

A 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 in Analytical Data Science, a core function within Product Development Data Sciences (PDD) that provides strategic leadership and scientific rigor across Development at Roche. PDD Analytical Data Science teams are mobilized across the portfolio to generate data-driven insights, identify opportunities for scale, and implement impactful solutions. PDD Analytical Data Science is recognized as a leading hub for top industry talent, operating as an agile workforce to deliver regulatory commitments across the portfolio. We identify, influence, and adopt industry-leading digital and automation solutions, develop analytical approaches to support exploratory analyses, and align statistical programming practices across both early- and late-stage clinical development. The Opportunity The Analytical Data Science Program Lead serves as a senior leader within the Analytical Data Science function, responsible for guiding both the technical strategy and operational execution across multiple clinical programs or an entire therapeutic area. This role leads a team of highly skilled programmers and junior leaders, ensuring the delivery of high-quality, regulatory-compliant analytical outputs that support key development milestones and health authority submissions. In addition to overseeing day-to-day delivery, the Analytical Data Science Program Lead is accountable for a broad range of analytical outputs including but not limited to: exploratory analyses, application development and dynamic visualization to enable ongoing data review and scientific insights generation. The Analytical Data Science Program Lead also oversees deliverables originating from cross-functional partners, such as Data Management, ensuring seamless integration into the reporting pipeline. The Analytical Data Science Program Lead sets priorities, allocates resources, and ensures the scalability and sustainability of programming operations through standardization, automation, and innovation, while providing business context to guide decision‑making with evolving portfolio needs. The Analytical Data Science Program Lead plays a pivotal role in cross‑functional planning and governance, acting as a strategic partner to stakeholders across PDD. As a people leader, the Analytical Data Science Program Lead is accountable for building and developing talent, fostering a culture of technical excellence, and ensuring alignment with both functional and enterprise‑wide data strategies. You define and drive the programming and analytical strategy across one or more clinical studies, ensuring alignment with clinical and regulatory objectives, accountable to the TA lead. You ensure compliance and inspection readiness by establishing robust quality review processes, maintaining thorough documentation, and proactively addressing potential risks to support internal audits and global health authority inspections. You drive and uphold data and programming standards by championing the consistent application of standardized methodologies, tools, and code libraries to ensure efficiency, reproducibility, and alignment with enterprise‑wide data strategy and regulatory expectations. You lead cross‑functional planning and execution of data and analytical deliverables, proactively anticipating risks and developing mitigation strategies to ensure quality, consistency, and timeliness. You act as a subject matter expert and best practices resource within programming, contributing to the development and refinement of functional standards, tools, and processes. You participate in global or complex initiatives, bringing analytical and programming expertise to solve problems spanning studies or functions. You contribute to the implementation of innovative approaches, including automation or new delivery models, to enhance efficiency and scalability. You collaborate with stakeholders across PDD, such as Biostatistics, Data Management, and Early Development Biometrics, to integrate analytical strategies into development plans and ensure alignment across the end‑to‑end drug development lifecycle. You share knowledge and lessons learned across programs and therapeutic areas to promote continuous improvement, cross‑team knowledge transfer, and enhance consistency in analytical approaches. You serve as a mentor to less experienced colleagues, promoting best practices in software development, analytics tooling, and scientific collaboration. Who you are You hold an advanced degree (Master’s or PhD) in Data Science, Statistics, Computer Science, Biomedical Informatics, or a related field. You have a minimum of 6 years of experience in pharmaceutical R&D or a regulated environment, with significant exposure to clinical development. You have demonstrated leadership of molecule‑level analytical strategy or delivery across multiple studies. You bring strong technical expertise in statistical programming (e.g., R, SAS), QC practices, and regulatory data standards (e.g., CDISC, ADaM, SDTM). You have a proven ability to manage complex timelines, collaborate across functions, and communicate analytical strategies effectively. You have experience in vendor oversight and working in matrixed, cross‑functional global teams. You demonstrate capacity for independent thinking and ability to make decisions based upon sound principles. You bring excellent strategic agility including problem‑solving and critical thinking skills, and agility that extends beyond the technical domain. You demonstrate respect for cultural differences when interacting with colleagues in the global workplace. You have excellent verbal and written communication skills, specifically in the areas of presentation and writing. Preferred Qualifications Experience leading submission activities or global programs. Demonstrated influence in cross‑functional or global team settings. Deep knowledge of the drug development lifecycle and how analytics supports key milestones. Relocation benefits are not available for this posting. The expected salary range for this position based on the primary location of Massachusetts is $136,400.00 - $253,200.00. 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. 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. 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