Senior Statistical Programmer (SAS + R) – Remote

Farmacia Con Atención Al Usuario Personalizada

Valladolid

Remote

EUR 90,000 - 130,000

Full time

4 days ago
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Job summary

Cytel Inc. seeks a Senior/Principal Statistical Programmer for remote work, embedded with a pharmaceutical client. You will independently lead programming efforts, develop SDTM/ADaM specifications, and deliver high‑quality datasets, tables, and figures.

Strong leadership and FDA/ICH knowledge are essential, with CRO oversight across multiple studies. The role requires 7+ years in biostatistics programming, proficiency in SAS and CDISC standards, and the ability to support regulatory submissions

Qualifications

  • Bachelor's degree in CS, data science, mathematics or statistics preferred.
  • 7+ years as Statistical Programmer in Biotech/Pharma
  • SAS programming with SDTM/ADaM guidelines and Define.xml experience
  • Experience supporting regulatory submissions with FDA/ICH familiarity
  • Ability to work independently and lead programming efforts with CROs

Responsibilities

  • Develop SDTM/ADaM specs, datasets, and define.xml for multiple studies.
  • Create SAS programs for datasets, listings, tables, and graphs.
  • Oversee CROs' programming deliverables to meet timelines.
  • Support regulatory submissions and study reports, DSURs, explorations analyses.
  • Contribute to programming standards and SOPs.

Skills

SAS programming
R programming
CDISC SDTM/ADaM
FDA/ICH regulatory knowledge
Regulatory submissions
Independent work
Leadership

Education

Bachelor's degree in CS/Data Science/Math/Statistics

Tools

Python
Java
Shiny
Unix/Linux
Git

Job description

Cytel Inc. seeks a Senior/Principal Statistical Programmer for remote work, embedded with a pharmaceutical client. You will independently lead programming efforts, develop SDTM/ADaM specifications, and deliver high‑quality datasets, tables, and figures.

Strong leadership and FDA/ICH knowledge are essential, with CRO oversight across multiple studies. The role requires 7+ years in biostatistics programming, proficiency in SAS and CDISC standards, and the ability to support regulatory submissions

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