Senior R Statistical Programmer

Cytel

$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 5 years' experience in pharma, biotech, or CRO
  • Expertise in R within regulated clinical development environments
  • Strong skills in R data manipulation using tidyverse
  • Proficient in R visualization for static outputs and dashboards
  • Experience in developing R packages with documentation and testing
  • Familiarity with SAS coding and SAS/MACRO preferred
  • Knowledge of Posit software suite (Workbench, Positron, Connect)
  • Attention to detail with ability to manage multiple priorities
  • Understanding of drug development life cycle and clinical trial data reporting
  • Effective communication in a global team setting

Responsibilities

  • Collaborate with teams to improve data processes and tools
  • Develop reusable R package code and provide training
  • Promote innovation in data analysis and visualization
  • Partner with study teams to enhance tools and processes
  • Facilitate change management and training for systems
Full Job Description
Job Description

The R Technical Solutions Programmer is responsible for implementing the vision for data and analysis infrastructure platforms and other technical solutions to support the data flow from data collection to data submission. Using expertise in R programming and clinical trials to create solutions that will enable an open-source ecosystem for programming. This role will coordinate gathering and prioritizing requirements in the process of design and delivery of fit-for-purpose data and analysis technical solutions.

Responsibilities

  • Collaborates with internal teams to understand requirements and develop processes, tools and utilities that will improve quality and efficiency
  • Develops reusable and robust R package code and/or utilities, along with detailed training/documentation
  • Promotes technical innovation to drive the development of data analysis and visualization solutions within a clinical data environment
  • Partners with study teams in use and further improvement of processes and tools
  • Facilitates change management activities and training for department systems and processes


Qualifications

  • Minimum 5 years' industry experience (Pharma, Biotech, CRO)
  • Experience with R within regulated clinical development environments
  • Strong R data manipulation and analysis skills using standard tidyverse packages
  • Strong R visualization skills for use in static outputs and dashboards
  • Experience with developing R packages including proper documentation and testing
  • Experience developing SAS code including SAS/MACRO preferred
  • Familiarity with Posit products including Workbench, Positron, and Connect
  • High attention to detail including proven ability to manage multiple, competing priorities
  • Familiarity with drug development life cycle and experience with manipulation, analysis, and reporting of clinical trials' data
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners

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