Principal Statistical Programmer - SAS + R (Remote)

Stor-Age Property Reit Limited

South Africa

Remote

ZAR 1,000,000 - 1,800,000

Full time

12 days ago

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Job summary

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to work remotely for a sponsor-dedicated project with one global pharmaceutical client. The role focuses on SAS and R programming, CDISC SDTM/ADaM, and regulatory submissions, with leadership responsibilities across CRO vendors.

You will work under the Director, Biostatistics and Programming, delivering high-quality data analyses, listings, and reports while ensuring compliance with FDA/ICH guidelines.

Qualifications

  • Bachelor’s degree in CS/Data Science/Math/Statistics.
  • 7+ years of experience as Statistical Programmer in Biotech/Pharma Clinical Development Biometrics Team.
  • Exceptional SAS programming skills and CDISC standards expertise.
  • Experience with regulatory submissions and FDA/ICH regulations.

Responsibilities

  • Generate SDTM, ADaM specifications, datasets, reviewer’s guide and Define.xml files for multiple studies.
  • Develop SAS programs to generate datasets, complex listings, tables and graphs.
  • Deliver high‑quality programming results including SAS and/or R programs tailored to clinical development programs.
  • Oversee CROs’ statistical programming deliverables to meet timelines and quality standards.
  • Support preparation of Clinical Study Reports, regulatory submissions and DSURs.

Skills

SAS programming
R programming
CDISC SDTM/ADaM
FDA/ICH regulations
Clinical development experience
Leadership / communication

Education

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

Tools

SAS
R
Unix/Git

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to work remotely for a sponsor-dedicated project with one global pharmaceutical client. The role focuses on SAS and R programming, CDISC SDTM/ADaM, and regulatory submissions, with leadership responsibilities across CRO vendors.

You will work under the Director, Biostatistics and Programming, delivering high-quality data analyses, listings, and reports while ensuring compliance with FDA/ICH guidelines.

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