Senior Clinical Data Scientist

Join to apply for theSenior Clinical Data Scientistrole atNanosep AB.

Responsibilities:

1. Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings).
2. Validate R packages.
3. Lead implementation in R and train other Biostatistics team members.
4. Create and validate safety and efficacy study outputs (e.g., ADaM, TLFs) in accordance with data definitions, specifications, and study documentation (protocol, SAP, aCRF).
5. Conduct statistical programming of clinical data using R.
6. Identify problems and develop tools to improve efficiency of the Statistical Programming group.
7. Collaborate with peers and statisticians to ensure quality and accuracy of clinical data submissions (e.g., SDTM, ADaM, tables, figures, listings, define.xml).

Qualifications:

• Minimum 5+ years of experience in R programming for clinical trials, including developing and validating R packages from CRO or pharmaceutical industry.
• Strong programming skills in R/R Shiny.
• Understanding of end-to-end clinical trial processes is mandatory.
• Experience with late-phase and RWE studies is desirable.
• Proven ability to apply R and R-Shiny for analysis and reporting, with skills in data visualization and wrangling.
• Knowledge of industry standards like CDISC data structures.
• Deep understanding of clinical trial phases and drug development process.

IQVIA is a leading provider of clinical research services and healthcare insights. Learn more athttps://jobs.iqvia.com.

We value diverse talent committed to innovation and impact. Join us to help improve patient outcomes worldwide.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

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