Genentech · 7 hours ago
Senior ADS Programmer
Boston, MA
Full-time
Onsite
Mid, Senior Level
$114K/yr - $212K/yr
5+ years expGenentech is committed to advancing science and ensuring access to healthcare. The Analytical Data Science Programmer plays a crucial role in transforming statistical analysis plans into high-quality programming deliverables, supporting regulatory submissions, and generating data insights for clinical programs.
BiotechnologyLife ScienceManufacturing
Responsibilities
You independently develop, validate, and maintain datasets and statistical outputs for clinical trials, including Study Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets, and tables, listings, and figures (TLFs), ensuring programming accuracy, traceability, and compliance with internal processes and regulatory expectations
You develop and support programming outputs across a wide range of data types, including exploratory biomarker data and real-world data, to support both regulatory and scientific objectives
You collaborate on exploratory analyses that span disease areas and therapeutic areas, enabling insight generation to inform drug development strategies
You support the creation and refinement of interactive tools and analytical applications (e.g., dashboards or visual data platforms) that enable dynamic exploration of integrated datasets by scientific and clinical teams
You provide programming leadership for assigned studies, coordinating deliverables across internal and external programming partners to meet study timelines and requirements
You interpret statistical analysis plans and translate them into executable programming specifications to ensure scientific rigor in outputs
You troubleshoot and resolve technical programming challenges with limited supervision, proactively identifying risks and implementing effective solutions while meeting timelines
You contribute to the design and maintenance of standard macros and reusable components, promoting efficiency and consistency across multiple studies and projects
You document programming workflows and maintain audit trails, ensuring study files are complete, traceable, and inspection-ready
You work cross-functionally with stakeholders, including biostatistics, data management, and clinical operations, to define programming timelines and deliverables
You engage in process improvement and innovation activities and participate in learning activities to grow knowledge of clinical research and programming standards
Qualification
Required
You hold a Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field
You have a minimum of 5 years of experience in statistical programming in a clinical development setting, or an advanced degree with 3 years of equivalent work experience
You are proficient in or have working knowledge of a modern programming language (such as SAS or R) and visualization/review tools
You have a deep understanding of statistical quality, endpoints, and QC processes
You have experience with Clinical Data Interchange Standards Consortium (CDISC) standards (e.g., SDTM and ADaM)
You bring expertise in handling and analyzing different types of data (multi-modal)
You have demonstrated ability to deliver programming outputs independently
You demonstrate respect for cultural differences when interacting with colleagues in the global workplace
You are fluent in English
Preferred
Possess attention to detail for regulatory submission processes and related documentation
Demonstrate critical thinking, strong organizational and problem-solving skills
Experience working in cross-functional global study teams
Effective communication skills with the ability to translate complex statistical concepts for non-statistical audiences
Experience with multiple phases of drug development (early and/or late stage)
Excellent communication skills, including the ability to influence and translate complex data for non-technical stakeholders
Demonstrated willingness to adapt, grow, and evolve in response to shifting priorities
Benefits
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.
Company
Genentech
Genentech is a biotechnology research company that specializes in genetic testing and personalized medicines.
10001+ employees
H1B Sponsorship
Genentech has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (148)
2023 (150)
2022 (178)
2021 (121)
2020 (158)
Funding
Current Stage
Public CompanyTotal Funding
unknown2009-03-26Acquired
1999-07-20IPO
1976-01-01Series Unknown
Leadership Team
Ashley Magargee
Chief Executive Officer
Michael Laird
Vice President, Global MSAT Drug Substance Biologics Technology and Commercial Products Support
Recent News
2026-01-23
Genetic Engineering News
2026-01-23
Company data provided by crunchbase