Senior Clinical Data Scientist

IQVIA Argentina; Reading; Hybrid; GBP 50,000 - 80,000; Full time

Job summary

A leading global provider of clinical research services is seeking a senior statistical programmer to develop and validate R packages for clinical trial analysis. The role requires a minimum of 5 years of experience in R programming, strong skills in data visualization, and a solid understanding of clinical trial methodologies. Join a team committed to improving patient outcomes through innovative medical treatments.

Qualifications

• Minimum 5+ years of experience in R programming for clinical trial data.
• Strong programming skills in R/R Shiny.
• Understanding of end-to-end Clinical Trials in Statistical Programming.

Responsibilities

• Develop internal and external R packages for clinical trial analysis.
• Validate R packages and lead implementation in R.
• Collaborate with peers to ensure quality and accuracy of clinical data.

Skills

R programming

Data visualization

Data wrangling

Statistical methodologies

Job description

Responsibilities

• Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings).

• Validate R packages.

• Lead implementation in R and train other Biostatistics team members.

• Create and validate safety and efficacy study output requirements (e.g., ADaM, TLFs) aligned with data definitions, specifications, and study documentation (e.g., protocol, SAP, aCRF).

• Conduct statistical programming of clinical data using R.

• Develop global tools to enhance the efficiency and capacity of the Statistical Programming group.

• Collaborate with peers and statisticians to ensure the quality and accuracy of clinical data for submission readiness (e.g., SDTM, ADaM, tables, figures, listings, define.xml).

Experience and Qualifications

• Minimum 5+ years of experience in R programming for clinical trial data, including developing and validating R packages from CRO or Pharmaceutical Industry.

• Strong programming skills in R/R Shiny.
• Understanding of end-to-end Clinical Trials in Statistical Programming is mandatory.
• Exposure to Late Phase & Real-World Evidence (RWE) studies is highly desirable.
• Proven experience in applying R and R-Shiny for clinical trial analysis and reporting. Ability to reproduce statistical analyses using R.
• Strong skills in data visualization and data wrangling with R, including using R packages for exploration and visualization.

• Knowledge of statistical methodologies in clinical trial analysis and experience with R-Shiny apps for data exploration.

• Advanced understanding of industry standards including CDISC data structures and standard program development.

• In-depth knowledge of clinical trial phases and drug development processes.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We facilitate connections to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com