Principal Statistical Programmer (Remote) - SAS + R Expert

Wrike

Islas Baleares

Remote

EUR 107,000 - 161,000

Full time

3 days ago
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Job summary

Cytel Inc. seeks a Senior/Principal Statistical Programmer SAS + R for a sponsor-dedicated role embedded with a pharmaceutical client. You will deliver SDTM/ADaM programming and oversee CRO deliverables, ensuring high-quality data outputs for regulatory submissions.

Requirements include a strong SAS and R skill set, extensive CDISC experience, and the ability to work independently with excellent communication and leadership capabilities.

Qualifications

  • Bachelor's degree in CS/DS/Math/Statistics required.
  • 7+ years of experience as Statistical Programmer in Biotech/Pharma.
  • Expert SAS programming skills and CDISC SDTM/ADaM proficiency.
  • Regulatory submission experience; ability to work independently.
  • Strong communication and leadership skills.

Responsibilities

  • Generate SDTM, ADaM specifications, datasets, reviewer’s guide and define.xml for multiple studies.
  • Develop SAS programs to create datasets, listings, tables and graphs.
  • Deliver high-quality programming results using SAS and/or R.
  • Oversee CRO deliverables for multiple studies.
  • Support clinical study reports, regulatory submissions, publications and DSUR.
  • Follow FDA regulations affecting reporting of trial data.
  • Develop and maintain standards for programming tools, outputs and macros.
  • Contribute to CRF edits, data validation plans and data transfer specs.
  • Collaborate to meet project timelines and goals; review SOPs/work instructions.

Skills

SAS programming
Data analysis
Leadership
Biostatistics

Education

Bachelor's degree in computer science, data science, mathematics, or statistics

Tools

SAS
R
CDISC (SDTM/ADaM)

Job description

Cytel Inc. seeks a Senior/Principal Statistical Programmer SAS + R for a sponsor-dedicated role embedded with a pharmaceutical client. You will deliver SDTM/ADaM programming and oversee CRO deliverables, ensuring high-quality data outputs for regulatory submissions.

Requirements include a strong SAS and R skill set, extensive CDISC experience, and the ability to work independently with excellent communication and leadership capabilities.

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