Scan your resume against ATS criteria for this Associate Director, Real-World Analytics Programming role at Revolutionmedicines.
Revolution Medicines is a global, commercial-state company dedicated to discovering, developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long-held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS-addicted cancers worldwide.
Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.
This position will serve as the lead statistical programmer for assigned real-world analytics and programming studies, independently managing programming activities from study initiation through final deliverables. The individual will be responsible for translating study protocols, statistical analysis plans (SAPs), and analysis specifications into high-quality, reproducible programming solutions and study outputs.
The Real-World Analytics Programmer will partner closely with HEOR/RWE scientists, data scientists, biostatisticians, and other cross-functional stakeholders to support the successful execution of observational research studies. The role requires strong technical expertise, attention to detail, and the ability to manage multiple studies and competing priorities in a fast-paced environment
Leads programming deliverables from study initiation through final report, including analysis dataset specifications, TLF shells, validation plans, programming documentation, and final study outputs.
Reviews and understand study-specific documents including protocols, SAPs, analysis specifications, and study concept documents to ensure accurate implementation of study requirements.
Translates study designs and analytic specifications into efficient, scalable, and reproducible programming solutions.
Independently develops, validates, and maintains SAS, SQL, R, Python, and other programming solutions for cohort construction, endpoint derivation, analysis dataset creation, and study deliverables.
Generates and quality-control analysis datasets, tables, listings, and figures (TLFs) in accordance with study protocols, SAPs, analysis specifications, and internal standards.
Supports a broad range of HEOR/RWE studies, including treatment pattern analyses, burden of illness studies, comparative effectiveness and safety studies, natural history studies, and external control arm analyses.
Implements and validate analytic methods specified in study protocols and SAPs, including survival analyses, propensity score approaches, confounding adjustment methods, and sensitivity analyses.
Works with multiple-focused real-world data assets, including claims, electronic health records (EHR), genomic testing databases, and linked clinical-genomic datasets.
Assesses data quality, completeness, and fitness-for-purpose and provide recommendations regarding data availability and implementation feasibility.
Independently performs quality control and validation activities for programming code, analysis datasets, and study outputs.
Develops and maintains technical documentation, programming specifications, reusable code, macros, and reproducible analytic workflows for assigned studies.
Collaborates closely with HEOR/RWE scientists, Data Scientists, and Biostatisticians to ensure accurate implementation of study methodologies and successful delivery of study objectives.
Communicates programming assumptions, implementation decisions, timelines, and risks to study teams and stakeholders.
Contributes to real-world programming standards, quality frameworks, and best practices.Provides technical guidance to junior programmers as appropriate.
Stays current with evolving industry best practices, technologies, and regulatory expectations related to real-world data and evidence generation.
BS/MS degree in Statistics, Biostatistics, Computer Science, Data Science, Epidemiology, Mathematics, or a related quantitative discipline.
8+ years of statistical programming experience in pharmaceutical, biotechnology, CRO, healthcare research, or related settings for Senior-level candidates.
Demonstrated experience independently leading programming activities for observational research, HEOR, epidemiology, or real-world evidence studies.
Strong SAS or R programming experience required, including experience developing analysis datasets and study deliverables from complex healthcare data sources.
Experience with SQL required and working knowledge of R or other programming language for data manipulation, analytics support, and quality control activities preferred.
Experience developing analysis datasets, tables, listings, and figures (TLFs) from complex healthcare or real-world data sources.
Experience working with large healthcare databases, including claims, EHR, genomic, registry, or linked clinical-genomic datasets.
Strong understanding of observational research workflows and implementation of study specifications.
Demonstrated ability to manage multiple projects simultaneously while meeting timelines and quality expectations.
Excellent written and verbal communication skills.
Strong analytical, problem-solving, and organizational skills with exceptional attention to detail.
Thrives in a collaborative team environment and is motivated to drive high-quality technical execution and continuous process improvement.
Oncology drug development or real-world evidence experience.
Experience working with major or healthcare real-world data assets, such as Flatiron Health, ConcertAI, COTA, Tempus, Guardant, Merative MarketScan, Komodo, Optum, TriNetX, or similar datasets.
Experience supporting HTA, market access, indirect treatment comparison (ITC), external control arm, or regulatory-grade real-world evidence studies.
Experience developing reusable programming frameworks, standardized macros, and validation tools.
Experience with Git, version control systems, and reproducible analytics workflows.
Experience working in a fast-paced and growing biotechnology organization.
#LI-VN1 #LI-Remote
The base pay salary range for this full-time position for candidates working at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.
Please note that base pay salary range is part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will collect, process and use any personal data that you provide to us in accordance with our https://www.revmed.com/ccpa-notice CCPA Notice and https://www.revmed.com/privacy-policy Privacy Policy. For additional information, please contact mailto:[email protected] [email protected].
Base Pay Salary Range$177,000—$221,000 USD
We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.
_ _
_Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official
email address._
_ _
_If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to
so we can share these impersonations with our IT team for tracking and awareness._
medical condition, and veteran status.
How to apply for Associate Director, Real-World Analytics Programming at Revolutionmedicines?
Click the "Apply on Company Website" button on this page to submit your application directly on the employer's official portal.
What is the salary for this role?
The salary for this role is $177,000 per annum.
What experience is required?
8+ years of experience is required.
Is this position still open?
Yes, currently active and accepting applications.
Explore related active roles in data_analytics
Associate Director, Real-World Analytics Programming
Revolutionmedicines · Remote (United States)
