Remote Principal Statistical Programmer (SAS + R)

Ledamc

Madrid

A distancia

EUR 90.000 - 130.000

Jornada completa

Hace 11 días

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Descripción de la vacante

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on a sponsor-dedicated program within a global pharmaceutical client. You will implement reporting and analysis activities for sponsor clinical trials and oversee CRO programmers to ensure high-quality data delivery.

The role requires extensive SAS programming, R programming experience, and strong knowledge of CDISC SDTM/ADaM standards with FDA/ICH regulations.

Formación

  • Bachelor's degree in computer science, data science, mathematics, or statistics.
  • 7+ years as a Statistical Programmer in Biotech/Pharma clinical development or similar.
  • Exceptional SAS programming skills and experience with clinical development data.
  • Extensive experience with CDISC SDTM/ADaM and Define.xml; FDA/ICH regulations.

Responsabilidades

  • Generate SDTM and ADaM specifications, datasets, and define.xmls for multiple studies.
  • Develop SAS programs to create datasets, listings, tables and graphs for clinical trials.
  • Lead high-quality statistical programming outputs and supervise CRO programmers.
  • Support regulatory submissions and clinical study reports; ensure timelines are met.

Conocimientos

SAS programming
Leadership
Independent work
Communication

Educación

Bachelor's degree in Computer Science/Data Science/Mathematics/Statistics

Herramientas

SAS
R
SDTM
ADaM
Define.xml

Descripción del empleo

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on a sponsor-dedicated program within a global pharmaceutical client. You will implement reporting and analysis activities for sponsor clinical trials and oversee CRO programmers to ensure high-quality data delivery.

The role requires extensive SAS programming, R programming experience, and strong knowledge of CDISC SDTM/ADaM standards with FDA/ICH regulations.

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