Principal Statistical Programmer (SAS/R) — Remote Lead

Recodme

Marbella

Remote

EUR 90,000 - 120,000

Full time

5 days ago
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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to work embedded with a pharmaceutical client, delivering sophisticated SAS and R programming for clinical trials. You will develop SDTM/ADaM datasets, define.xml, and supportive tables and figures while coordinating with CROs to ensure timely, high-quality outputs.

The role emphasizes regulatory-compliant programming, collaboration with biostatistics and programming leadership, and contributing to study reports and submissions

Qualifications

  • Senior-level statistical programming experience in clinical trials.
  • Experience with SDTM/ADaM datasets and define.xml.
  • Familiarity with FDA regulations and eCTD submissions.

Responsibilities

  • Generate SDTM, ADaM specs, datasets, reviewer''s guide and define.xml for multiple studies.
  • Develop SAS programs for datasets, listings, tables, and graphs.
  • Deliver high-quality SAS/R programs tailored to development needs and timelines.
  • Oversee CRO programming deliverables across studies to ensure quality and timeliness.
  • Support preparation of reports, regulatory submissions, and exploratory analyses.

Skills

SAS programming
R programming
Clinical trials
Statistical analysis
CRO oversight

Tools

SAS
R

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to work embedded with a pharmaceutical client, delivering sophisticated SAS and R programming for clinical trials. You will develop SDTM/ADaM datasets, define.xml, and supportive tables and figures while coordinating with CROs to ensure timely, high-quality outputs.

The role emphasizes regulatory-compliant programming, collaboration with biostatistics and programming leadership, and contributing to study reports and submissions

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