IQVIA
life sciences
PrincipalStatisticalProgrammer(PK/PD)(m/w/d)
“Principal Statistical Programmer (PK/PD) (m/w/d) at IQVIA. Skills: SAS programming, CDISC standards, PK/PD analysis. Lead development and validation. Design and implement PK/PD datasets”
What You'll Achieve.
enhance efficiency and quality; support early-phase decision-making; support integrated analyses
Industry & Context.
What They're Looking For.
Must Have
SAS programming, CDISC standards, SDTM, ADaM, TLF generation, Safety datasets, PK and PK/PD ADaM datasets, PopPK / PK/PD / Exposure–Response workflows, early-phase clinical trial designs, Phase / First-in-Human (FIH) studies, Crossover studies, Exposure–response analysis, PK parameter pooling, Lead Programmer or Technical Lead experience, regulatory submissions
Nice to Have
Translational Medicine or Clinical Pharmacology functions support, exploratory analyses, early-phase clinical decision-making, integrated summaries, pooled PK analyses across studies, cross-functional collaboration in drug development environments
What You'll Do.
Lead development and validation
Design and implement PK/PD datasets
Support PopPK / PK/PD / ER analyses
Provide programming leadership
Contribute to regulatory submissions
Develop standard programming practices
Ensure adherence to timelines
How You'll Work.
Team & Collaboration
Collaborate with Clinical Pharmacology, Biostatistics, and Translational Medicine teams; cross-functional collaboration
Communication Scope
communication
Process & Methodology
guiding project delivery, manage multiple priorities
Applying for this Principal Statistical Programmer (PK/PD) (m/w/d) role?
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