Senior Statistical Programmer

Hace 5 días

Barcelona, Cataluña, España Jobrapido Jornada completa
OverviewCompruebe que cumple con los requisitos de habilidades para este puesto, así como con la experiencia asociada, y luego envíe su CV a continuación.

In this role, you will lead the design, development, and QC of SAS programs to create ADaM datasets, tables, figures, and submission packages. You collaborate with study teams to ensure submission-ready data (SDTM/ADaM) and oversee complex analyses and data delivery for regulatory submissions. You will drive efficiency by developing global tools and leading programming activities across multiple studies. This is a hands-on, impact-oriented position within a cross-functional environment that shapes how data supports regulatory decisions and publications.

Responsabilidades
  • Design data structure and specifications for ADaM datasets, tables, figures, listings, and submission content
  • Ensure submission readiness and data quality for SDTM, ADaM, tables, figures, listings, and define.xml
  • Lead pooled and exploratory analyses, working with statistics leads and programming teams
  • Oversee ISS and ISE dataset specification and delivery when not provided by CRO
  • Design and implement complex SAS programs for CDISC ADaM data analysis and reporting
  • Develop global tools to improve efficiency and capacity of the Statistical Programming group
  • Coordinate with study teams to meet timelines and deliver high-quality outputs
  • Collaborate with CR&D for data analysis requests; support regulatory responses, integrated summaries, publications, and exploratory analyses of available data
Requisitos principales
  • 5+ years in clinical programming and/or statistical programming in CRO/pharmaceutical environments
  • Deep understanding of clinical programming processes and standards
  • Extensive SAS programming experience including SAS Macros xkdbapo
  • Strong programming and problem-solving skills
  • Proficient in R programming (hands-on)
  • Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM)
  • Proven experience leading programming activities for pooled and exploratory analyses across multiple studies
  • Ability to work independently or in teams and manage timelines
  • Experience in cross-functional, multicultural, international clinical trial teams
  • collaboration
  • communication
  • problem-solving
  • SAS programming
  • SAS Macros
  • R programming