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Assistant R Statistical Programmer Jobs in Massachusetts

Vrtx

Principal Biostatistician

Boston, MA · Hybrid

$174K - $262K/yr

Develops breadth of knowledge across related disciplines with a drug developer mindset. Knowledge and Skills: In-depth experience with SAS and R statistical software Demonstrated understanding of ...

AstraZeneca

Head of Statistical Programming

Boston, MA · On-site

This role leads the statistical programming function at enterprise scale-defining how data ... Delivery of continuous improvement and large-scale change projects within the function or across R ...

AstraZeneca

Head of Statistical Programming

Boston, MA · On-site

This role leads the statistical programming function at enterprise scale-defining how data ... Delivery of continuous improvement and large-scale change projects within the function or across R ...

Cytel

Principal Biostatistician FSP

Cambridge, MA · On-site +1

Knowledge and implementation of advanced statistical methods. * Good SAS and R programming skills for QCing critical outputs, Efficacy/Safety tables and working closely with Programmers. Knowledge of ...

MMS

Study Design Statistician (US)

Boston, MA · On-site

Our experienced statisticians and programmers develop intellectual property and assets to support ... Experience in SAS and/ or R statistical software packages. * Experience in study design and ...

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Assistant R Statistical Programmer information

What is the difference between Assistant R Statistical Programmer vs Data Analyst?

AspectAssistant R Statistical ProgrammerData Analyst
Required SkillsProficiency in R, basic statistical knowledge, programming skillsData manipulation, visualization, statistical analysis, often using R or Excel
Work EnvironmentClinical research, pharmaceutical, or biotech industriesBusiness, marketing, finance, healthcare sectors
CertificationsOften requires a degree in statistics, biostatistics, or related fieldsDegree in statistics, data science, or related fields; certifications like CAP or Microsoft certifications are common

While both roles involve data analysis and programming skills, the Assistant R Statistical Programmer primarily supports clinical trials and pharmaceutical research, focusing on statistical programming in R. Data Analysts work across various industries analyzing data to inform business decisions. The roles share similar educational backgrounds but differ in industry focus and specific job functions.

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Assistant R Statistical Programmer jobs near you
Associate Director, Statistical Programming

Associate Director, Statistical Programming

MapLight Therapeutics

Burlington, MA • Hybrid

Other

Re-posted 2 days ago

Job description

What You'll Do: Reporting to the Senior Director, Statistical Programming, the Associate Director will provide statistical and clinical data programming expertise to manage statistical programming activities that support drug development programs and regulatory submissions. This role involves overseeing the creation, validation, and delivery of programming deliverables, ensuring compliance with industry standards, and fostering cross-functional collaboration with biostatistics, data management, clinical, and regulatory teams.

Responsibilities: 

  • Oversee the development and validation of SAS programs to generate datasets (SDTM, ADaM), tables, listings, and figures (TLFs) in compliance with CDISC standards.
  • Ensure the timely and high-quality delivery of programming outputs for regulatory submissions, clinical study reports, and exploratory analyses.
  • Ensure all programming activities align with industry standards (CDISC, ICH, FDA, EMA) and internal SOPs.
  • Programming lead for clinical programs as needed. Hand-on programming work in SAS and other programming languages/tools.
  • Establishes and maintains CRO/vendor partnerships.
  • Act as a liaison between statistical programming and other functions, ensuring clear communication and alignment of goals.
  • Partner with biostatistics, data management, and clinical operations to resolve programming issues and optimize processes.
  • Identify and implement new tools, techniques, and processes to improve efficiency and quality in statistical programming.

Qualifications:

  • Master's degree in statistics, computer science or a related field
  • At least 8 years of statistical programming experience in the pharmaceutical/biotech industry
  • Proven ability to manage CRO relationships and oversee programmed deliverables.
  • Extensive experience in leading statistical programming function for both early and late phase clinical trials, and regulatory submissions (NDA/BLA, MAA)
  • Excellent skills in SAS programming and statistical reporting, knowledge of R and R Shiny desirable
  • In-depth knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements
  • Familiarity with FDA and ICH regulations and guidelines
  • Excellent written and verbal communication skills, ability to collaborate with a multidisciplinary team and interact effectively in a fast-paced team environment

Location: This is a hybrid role with three days per week in-office in Burlington, Massachusetts.

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