DSX Data Scientist (On Site, Clinical Trial Data, CSRs) at F. Hoffmann-La Roche Ltd - Poland

South San Francisco, California, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Feb, 26

Salary

200000.0

Posted On

23 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Science, Statistical Computing, Software Engineering, Programming, Automation, Data Visualization, Clinical Trial Data, R, Python, Git, Docker, Bioinformatics, Problem-Solving, Critical Thinking, Collaboration, Communication

Industry

Biotechnology Research

Description

DSX Data Scientist (On Site, Clinical Trial Data, CSRs) Department Summary 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 Data Scientist in the Data Science Acceleration (DSX) team is responsible for developing scalable tools, environments, and workflows that enable efficient, high-quality statistical computing across Product Development Data Sciences (PDD). This role focuses on creating and maintaining next-generation capabilities that support automation of programming workflows, generation of reusable coding macros, and advanced data visualization. Working closely with statistical programmers, biostatisticians, and clinical scientists, the Data Scientist translates scientific and operational needs into robust, modular, and user-friendly solutions that streamline evidence generation and support faster, more reliable decision-making across the development pipeline. You contribute to the design, development, and maintenance of statistical computing environments and tools that enable efficient analysis of clinical and operational data. You develop and implement reusable code libraries, macros, and automation pipelines to support programming workflows across PDD. You collaborate with statisticians, programmers, and data scientists to translate user needs into robust, scalable technical solutions. You support exploratory analytics and data visualization capabilities that enhance insight generation and decision-making across development programs. You apply software engineering best practices, including version control, testing, and documentation, to ensure high-quality, reproducible code. You participate in the continuous improvement of DSX tools and infrastructure, incorporating feedback and emerging technologies. You support regular review of opportunities to simplify and innovate, and collaborate with experts in PDD and beyond to accelerate and deliver patient benefits faster. You work under general supervision and apply independent judgment to interpret guidance, prioritize responsibilities, and make decisions in situations that require contextual understanding. You apply judgment to address moderately complex statistical or data issues, balancing scientific rigor with appropriate flexibility, and seek guidance when facing novel or ambiguous situations. You adhere to functional standards by participating in peer review and mentoring relationships to uphold quality and build methodological and programming expertise. Who You Are You hold a Master’s degree or PhD in Computer Science, Data Science, Statistics, Bioinformatics, Engineering, or a related quantitative discipline. You have 2+ years of hands-on experience in data science, statistical computing, software engineering, or a related field, preferably in a life sciences or healthcare setting (internship and academic experience will be considered). You are proficient in programming languages commonly used in statistical computing (e.g., R, Python) and are familiar with development tools such as Git, Docker, or workflow automation tools. You understand clinical trial data structures, statistical analysis concepts, or biomedical data (e.g., omics, real-world data, operational data). You demonstrate ability to build, test, and maintain reproducible, well-documented code. 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, with the ability to explain complex technical concepts in clear language. Preferred Qualifications Experience working with diverse data modalities (e.g., clinical, operational, real-world, omics) and applying analytical strategies to uncover patterns or insights. Familiarity with statistical computing workflows in regulated environments, including clinical trial data structures and lifecycle. Demonstrated interest in data engineering best practices (e.g., reproducibility, code modularity, testability, documentation). Ability to follow and contribute to collaborative development processes, including code reviews, version control, and continuous integration. Experience contributing to the development or extension of statistical platforms, macro libraries, or reusable toolkits. Strong communication and collaboration skills, with the ability to translate user needs into technical requirements and explain complex solutions in accessible terms. Exposure to automation, workflow orchestration tools (e.g., Airflow, Nextflow), or containerization (e.g., Docker, Kubernetes) is a plus. Experience working in multi-disciplinary or matrixed R&D teams, preferably within a global pharmaceutical or biotech organization. Relocation benefits are not available for this posting. The expected salary range for this position based on the primary location of California is $122,300.00 and $200,000.00. 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 #PDDSSF 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. Who We Are Genentech, a member of the Roche group and founder of the biotechnology industry, is dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. To solve the world's most complex health challenges, we ask bigger questions that challenge our industry and the boundaries of science to transform society. Our transformational discoveries include the first targeted antibody for cancer and the first medicine for primary progressive multiple sclerosis. The next step is yours. To apply today, click on the "Apply for this job" button. 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.

Responsibilities

The Data Scientist is responsible for developing scalable tools and workflows for efficient statistical computing across Product Development Data Sciences. This role involves collaborating with various teams to translate scientific needs into robust solutions that enhance decision-making in clinical development.