7 Apr 2026

R Programming Lead (Statistical Programming)

IQVIA

Amsterdam

7 Apr 2026

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R Programming Lead role in a sponsor-dedicated team, focusing on clinical trial analysis using R and R-Shiny. Responsibilities include developing R packages, building applications, and leading statistical programming efforts. Requires strong R programming experience in the pharmaceutical or CRO industry.

RemoteFull-timeLeadR ProgrammingR Packages

R Programming Lead (Statistical Programming)

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RemoteFull-timeLeadR Programming

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

Remote

Employment Type

Full-time

Experience Level

Strong experience in R programming for clinical trial data

Core Qualifications

Technical (Must-have)

R programmingR packagesR-ShinyCDISCADaMSDTMStatistical programmingData visualizationData wranglingClinical trial analysis

Soft Skills

LeadershipTrainingCollaborationProblem solvingQuality assurance

Tools (Must-have)

RR-Shiny

Preferred Qualifications

Technical (Nice-to-have)

Late PhaseReal-World Evidence (RWE)Global Medical Affairs

Key Responsibilities

•Develop internal and external R packages for clinical trial analysis (ADaM, tables, figures, listings)
•Validate R packages
•Building complex R-Shiny applications (animations, dashboards) to address clinical questions, EU JCA requirements, and decision-making
•Lead implementation in R and train other Biostatistics team members
•Conduct statistical programming work of clinical data using R
•Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group
•Create and/or validate all safety and efficacy study output requirements (e.g. ADaM, TLFs) consistent with data definitions and specifications and relevant study documentation (e.g. protocol, SAP, aCRF)
•Collaborates with peers and statisticians to ensure the quality and accuracy –thus submission readiness –of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml)

R ProgrammingStatistical ProgrammingClinical TrialPharmaceuticalHealthcareRemoteFull-timeLeadR-ShinyCDISC

Key Responsibilities

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

•Validate R packages

•Building complex R-Shiny applications (animations, dashboards) to address clinical questions, EU JCA requirements, and decision-making

•Lead implementation in R and train other Biostatistics team members

•Conduct statistical programming work of clinical data using R

•Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group

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

•Collaborates with peers and statisticians to ensure the quality and accuracy –thus submission readiness –of clinical data as required by authorities (i.e. SDTM, ADaM, tables, figures, listings, define.xml)