Senior Principal Statistical Programmer (SAS + R) - Remote

Farmatalent

Ribamontán al Mar

Remote

EUR 70,000 - 110,000

Full time

4 days ago
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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on global pharma clinical development projects. The role focuses on SAS and R programming, SDTM/ADaM specifications, and oversight of CRO programming deliverables.

You will contribute to regulatory submissions and complex data analyses while maintaining high-quality standards. The position requires 7+ years in the field, deep regulatory knowledge, and strong leadership and communication skills.

Qualifications

  • 7+ years of experience as a Statistical Programmer in Biotech/Pharma clinical development
  • Expert SAS programming with SDTM/ADaM/Define.xml implementation
  • Experience with FDA/ICH regulation and regulatory submissions
  • Ability to work independently and lead CRO collaborations
  • Strong written and verbal communication and leadership skills

Responsibilities

  • Generate SDTM, ADaM specifications, datasets, reviewers' guides and define.xml files for multiple studies
  • Develop SAS programs to generate datasets, complex listings, tables and graphs
  • Deliver high-quality SAS/R outputs tailored to clinical development needs
  • Oversee CRO programmers to ensure data delivery meets timelines
  • Support preparation of CSR, regulatory submissions, publications, DSUR and analyses
  • Contribute to standards for programming tools, outputs and macros

Skills

SAS programming
CDISC standards
Leadership
Communication

Education

Bachelor's degree in CS/Math/Stats

Tools

R
Python
Unix/Linux
Git

Job description

Cytel is seeking a Senior/Principal Statistical Programmer to work remotely on global pharma clinical development projects. The role focuses on SAS and R programming, SDTM/ADaM specifications, and oversight of CRO programming deliverables.

You will contribute to regulatory submissions and complex data analyses while maintaining high-quality standards. The position requires 7+ years in the field, deep regulatory knowledge, and strong leadership and communication skills.

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