Principal Statistical Programmer – SAS + R (Remote)

Pwc South Africa

East London

Remote

ZAR 900,000 - 1,200,000

Full time

12 days ago

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Job summary

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to work remotely with a global pharmaceutical client. The role focuses on SAS and R programming, SDTM/ADaM specifications, and regulatory submissions with minimum supervision and strong leadership expectations.

Ideal candidates have 7+ years in clinical development biometrics, excellent communication, and experience overseeing CRO programming deliverables. Remote setup supports across international teams.

Qualifications

  • Bachelor's degree in computer science, data science, mathematics, or statistics preferred.
  • 7+ years of Statistical Programmer experience in Biotech/Pharma Clinical Development or similar team.
  • Strong SAS programming skills and experience with SDTM/ADaM/Define.xml.
  • Familiarity with FDA/ICH regulations and regulatory submissions.
  • Ability to work independently and lead across CROs and internal teams.

Responsibilities

  • Generate SDTM and ADaM specifications and datasets, reviewer's guide and define.xml for multiple studies.
  • Develop SAS programs to produce datasets, listings, tables and graphs; collaborate with statisticians.
  • Deliver high-quality programming outputs and maintain SAS/R programs for clinical programs.
  • Oversee CRO programming deliverables to ensure timelines and quality.
  • Support preparation of CSRs, regulatory submissions and exploratory analyses.

Skills

SAS programming
R programming
CDISC SDTM/ADaM/Define.xml
FDA/ICH regulation
Independent working
Leadership
Communication (written and verbal)

Education

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

Tools

SAS
R
Python
Unix/Linux

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to work remotely with a global pharmaceutical client. The role focuses on SAS and R programming, SDTM/ADaM specifications, and regulatory submissions with minimum supervision and strong leadership expectations.

Ideal candidates have 7+ years in clinical development biometrics, excellent communication, and experience overseeing CRO programming deliverables. Remote setup supports across international teams.

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