IQVIA Argentina
Location
Reading, Berkshire | United Kingdom
Job description
Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced R programmer needed to provide technical expertise for Biostatistics department to meet internal and external needs. Lead the sponsors Biostatistics group R implementation team.
Prior experience with R package development and validation is required. Also, knowledge in clinical data standards (CDISC) is required.
• 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.
• 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).
Qualifications:
• Approximately 5 years or more in R programming for clinical trial data (Tidyverse, etc.), including developing and validating R packages.
• Bachelor’s degree in Math, Stats, Computer Science or similar
• Git/GitHub knowledge
• Knowledge of pharmaceutical clinical development (i.e. understanding of safety deliverables and efficacy analysis supporting regulatory submissions)
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at
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