Senior Principal Statistical Programmer (SAS + R) - Remote

Fundación Hospitalarias Comunidad De Madrid

Cáceres

Remote

EUR 85,000 - 116,000

Full time

4 days ago
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Job summary

Cytel Inc. is seeking a Senior/Principal Statistical Programmer SAS + R to join a sponsor-dedicated program, fully remote. You will generate SDTM/ADaM, develop SAS and R code, and oversee CROs to ensure high-quality data for multiple clinical trials.

The role requires 7+ years in biotech/pharma, expert SAS, CDISC, and familiarity with FDA/ICH guidelines, with strong communication and leadership skills to drive successful regulatory submissions.

Qualifications

  • 7+ years as a Statistical Programmer in Biotech/Pharma.
  • Expert SAS programming and SDTM/ADaM knowledge.
  • Experience supporting regulatory submissions and FDA/ICH guidelines.

Responsibilities

  • Generate SDTM, ADaM specs, datasets, define.xml and reviewer’s guide.
  • Develop SAS/R programs for tables, listings and figures; create complex graphs.
  • Coordinate with CROs to ensure timelines and quality across studies.
  • Contribute to regulatory submissions, publications and DSURs.

Skills

SAS programming
R programming
CDISC SDTM/ADaM
Regulatory submissions
Clinical development
Communication skills

Education

Bachelor's degree in Computer Science/Statistics/Mathematics

Tools

SAS
R
Python
Unix/Linux
Git
Shiny

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer SAS + R to join a sponsor-dedicated program, fully remote. You will generate SDTM/ADaM, develop SAS and R code, and oversee CROs to ensure high-quality data for multiple clinical trials.

The role requires 7+ years in biotech/pharma, expert SAS, CDISC, and familiarity with FDA/ICH guidelines, with strong communication and leadership skills to drive successful regulatory submissions.

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