Remote Principal Statistical Programmer (SAS + R)

Heineken

Stellenbosch

Remote

ZAR 1,488,000 - 2,479,000

Full time

9 days ago

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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely within a sponsor-driven environment. You will work on clinical development programs, generating SDTM/ADaM outputs and leading CRO programming efforts to ensure high-quality data delivery.

The role requires extensive SAS expertise, CDISC standards knowledge, and experience with regulatory submissions. You will collaborate with biostatistics and programming leadership to drive data quality and timely delivery

Qualifications

  • At a minimum bachelor's degree in computer science, data science, mathematics, or statistics.
  • 7+ years of experience as a Statistical Programmer on a Biotech/Pharma Clinical Development Biometrics Team or similar.
  • Exceptional SAS programming skills with clinical development experience.
  • Extensive applied experience of CDISC standards (SDTM, ADaM, Define.xml) and FDA/ICH regulation.
  • Experience supporting regulatory submissions and interactions with FDA/global authorities.

Responsibilities

  • Generate SDTM, ADaM specifications, datasets, reviewer's guides and define.xml for multiple studies.
  • Develop SAS programs to generate datasets, listings, tables, and graphs.
  • Deliver high-quality statistical programming results using SAS/R programs.
  • Oversee CRO programmers to ensure timely, high-quality outputs for multiple studies.
  • Support preparation of CSRs, regulatory submissions, publications, and exploratory analyses.

Skills

SAS programming
CDISC SDTM/ADaM
R programming
Regulatory submissions

Education

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

Tools

SAS
R
Python
Unix/Linux
Git

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely within a sponsor-driven environment. You will work on clinical development programs, generating SDTM/ADaM outputs and leading CRO programming efforts to ensure high-quality data delivery.

The role requires extensive SAS expertise, CDISC standards knowledge, and experience with regulatory submissions. You will collaborate with biostatistics and programming leadership to drive data quality and timely delivery

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