Associate Director, Real-World Analytics Programming

revolutionmedicines

EE. UU.

A distancia

USD 186.000 - 233.000

Jornada completa

14 días+

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Ventajas ofrecidas por este puesto de trabajo

Equity awards
Learning and development
Strong benefits

Descripción de la vacante

Revolution Medicines is seeking an Associate Director-level Statistical Programmer for Real-World Analytics in oncology. You will lead programming for observational studies, translating study designs into reproducible analysis solutions.

The role requires collaboration with HEOR/RWE scientists, data scientists, and biostatisticians to deliver high-quality outputs. You will develop, validate, and maintain SAS, SQL, R, Python code, and contribute to standards while mentoring junior programmers in

Formación

  • Significant experience as a statistical programmer for real-world evidence or observational studies.
  • Proficiency in SAS, SQL, R, Python for analysis-grade code development and validation.
  • Experience with oncology real-world data and analytic methods is preferred.

Responsabilidades

  • Lead programming for assigned real-world observational studies from kickoff to delivery.
  • Create analysis datasets, TLF shells, validation plans, and final study outputs.
  • Develop scalable, reproducible code and validate results across SAS/SQL/R/Python.
  • Collaborate with HEOR/RWE scientists, data scientists and biostatisticians.
  • Mentor junior programmers and contribute to programming standards.

Herramientas

SAS
SQL
R
Python
Survival analysis
Propensity scores
Version control (Git)
Data quality assessment

Descripción del empleo

Role overview

An Associate Director-level statistical programming role within Real-World Analytics, serving as the lead statistical programmer for assigned observational research studies in oncology. The position partners closely with HEOR/RWE scientists, data scientists, and biostatisticians to translate study protocols and analysis specifications into reproducible, high-quality programming solutions. It is well suited to a senior programmer who can manage multiple studies in a fast-paced, science-driven environment.

Responsibilities
  • Serve as the lead statistical programmer for assigned real-world studies, managing programming activities from study kickoff through final delivery.
  • Lead deliverables including analysis dataset specifications, TLF shells, validation plans, programming documentation, and final study outputs.
  • Translate study designs and analytic specifications into efficient, scalable, and reproducible programming solutions, including cohort construction, endpoint derivation, and analysis dataset creation.
  • Develop, validate, and maintain SAS, SQL, R, Python, and other programming solutions, and generate and quality-control analysis datasets, tables, listings, and figures.
  • Work with multiple oncology-focused real-world data assets, including claims, electronic health records, genomic testing databases, and linked clinical-genomic datasets.
  • Contribute to real-world programming standards, quality frameworks, and best practices, and provide technical guidance to junior programmers as appropriate.
Requirements
  • Significant experience as a statistical programmer supporting real-world evidence, HEOR, or observational research studies.
  • Strong proficiency in SAS, SQL, R, and Python, with the ability to independently develop, validate, and maintain analysis-grade code.
  • Deep understanding of oncology-relevant analytic methods such as survival analyses, propensity score approaches, confounding adjustment, and sensitivity analyses.
  • Experience assessing data quality, completeness, and fitness-for-purpose across claims, EHR, and clinical-genomic datasets.
  • Familiarity with version control tools such as Git and reproducible analytics workflows.
  • Experience developing reusable programming frameworks, standardized macros, and validation tools, ideally in a fast-paced and growing biotechnology organization.
Benefits and work setup
  • Remote work setup with a base pay salary range of $186,000 to $233,000 USD for candidates working onsite at the Redwood City, CA headquarters, adjusted for local market based on role, level, and location.
  • Total rewards package that includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.
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