Principal Statistical Programmer - SAS/R, Remote

Unifi Africa

Stellenbosch

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 (SAS + R) to be remote and work on sponsor-dedicated projects with a global pharma client, under Cytel's support.

You will lead programming activities, generate SDTM/ADaM, define.xml, support regulatory submissions, oversee CROs, ensure data quality, and contribute to standards.

Applicants should have 7+ years experience and strong communication; independent work style. This role offers remote work with international collaboration.

Qualifications

  • Bachelor's degree in CS, data science, math, or statistics.
  • 7+ years of statistical programming in biotech/pharma.
  • Expert SAS programming and clinical programming processes.
  • Extensive CDISC SDTM/ADaM/Define.xml experience.
  • Experience supporting regulatory submissions with FDA/ICH.
  • Ability to work independently.
  • Excellent written and verbal communication and leadership.

Responsibilities

  • Generate SDTM/ADaM specs, datasets, and define.xmls for multiple studies.
  • Develop SAS programs for datasets, listings, tables, and graphs.
  • Deliver high-quality programming outputs and validate scripts.
  • Oversee CRO programmers to meet timelines.
  • Support clinical study reports and regulatory submissions.
  • Ensure compliance with FDA/ICH regulations and GCP.
  • Contribute to standards, SOPs, and data validation plans.
  • Collaborate with CROs, vendors, and clinical partners.

Skills

SAS programming
R programming
CDISC standards (SDTM/ADaM/Define.xml)
FDA/ICH regulatory submissions
Independent work / leadership
Communication skills
CRO oversight

Education

Bachelor's degree in Computer Science, Data Science, Mathematics, or Statistics

Tools

Python
Java
Shiny
Unix/Linux
Git
Markdown

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to be remote and work on sponsor-dedicated projects with a global pharma client, under Cytel's support.

You will lead programming activities, generate SDTM/ADaM, define.xml, support regulatory submissions, oversee CROs, ensure data quality, and contribute to standards.

Applicants should have 7+ years experience and strong communication; independent work style. This role offers remote work with international collaboration.

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