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Senior Manager, Scientific Programming

BeiGene
United Statesfull_timeVerifiedPosted 27 Mar 2026
💰 $189,400/yr($144,400/yr$189,400/yr)

About the role

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Position Summary:

We are seeking a highly skilled Real-World Data (RWD) Programmer to join the Scientific Programming team. The successful candidate will lead programming activities to support real-world evidence (RWE) generation using large-scale healthcare data sources (e.g., electronic health records, claims, registries). This role will collaborate with biostatistics and technical teams to implement and deliver high-quality analytic datasets, outputs, and visualizations.

                                                                   

Essential Duties & Responsibilities:

  • Develop, validate and maintain analysis-ready datasets, tables, figures and listings for observational and RWE studies derived from diverse real-world data sources, including claims, electronic health records (EHRs) and registry data

  • Write, test and validate programs to produce analysis datasets, TLFs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed

  • Conduct exploratory data analyses to support evidence generation, feasibility assessments and study design refinement

  • Interact and communicate with programming teams and stakeholders to identify efficient programming solutions and contribute to analytic strategy

  • Manage and contribute to the standardization and automation of data processing workflows, including the development of reusable programming templates and data refreshes

  • Design and develop effective visualizations and interactive dashboards (e.g. Power BI, Spotfire, R-Shiny) to support decision-making

  • Apply best practice in RWD programming and analytics to develop and deliver high-quality reports independently

  • Understand and execute department-, product- and study-level macros and utilities. Write, test and validate product- and study-level macros and utilities

  • Be a technical resource for programming teams to provide advice on complex programming tasks and/or standards

  • Contribute to the development review of Statistical Programming policies, standard operating procedures and other controlled documents

  • Interface with outsourcing partners and vendors

  • Other duties as assigned

Core Competencies, Knowledge and Skill Requirements:

  • Strong proficiency in R and SQL (Python and SAS experience a plus) or other data manipulation languages to manage and analyze large-scale healthcare datasets.

  • Basic knowledge of statistical analysis methodologies and study design concepts

  • Fundamentals of project planning and management

  • Drug development process

Communication & Interpersonal Skills:

  • Excellent verbal and written communication skills

  • Excellent problem-solving skills and ability to work independently and collaboratively in a fast-paced environment

  • Ability to effectively collaborate in a dynamic environment

DESIRED BACKGROUND AND EXPERIENCE (Include License or Certifications)

  • Expert level R and SQL programmer with demonstrated experience in handling large-scale healthcare datasets and delivering on complex programming assignments and analysis

  • Deep knowledge of real-world data sources (claims, EHRs, registries) and observational study design

  • Strong understanding of healthcare coding systems (ICD, CPT, NDC, HCPCS, RxNorm)

  • Experience in supporting HEOR, epidemiology or medical affairs teams

  • Experience in Oncology studies

  • Experience leading or working with centralized teams for Statistical Programming

  • Experience in FDA/EMEA/CFDA trial and regulatory submissions

  • Experience in development and implementation of statistical programming standards and procedures

  • Experience with the drug development process (pre-, early, late and/or observational) in related industries or academic research. Experience with oncology trials.

  • Expert level SAS programmer with experience in delivering complex programming assignments and analysis. Proficient in developing their own code as well as modifying existing code.

REQUIREMENTS

Education:

  • Master’s degree, in Computer Science, Statistics, Mathematics, Life Sciences or o

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Company

BeiGene

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