Principal Statistical Programmer - SAS & R (Remote)

Placements24; South Africa; A distancia; ZAR 900.000 - 1.200.000; Jornada completa

Descripción de la vacante

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely on sponsor-dedicated projects with global pharmaceutical clients.

You will implement reporting and analysis activities, oversee CRO programmers, and ensure high-quality data outputs while adhering to FDA/ICH regulations. The role requires independent work, extensive SDTM/ADaM experience, and strong communication and leadership skills.

Formación

• Minimum bachelor’s degree in computer science, data science, mathematics, or statistics (preferred).
• 7+ years as Statistical Programmer in biotech/pharma clinical development biometrics.
• Strong SAS programming expertise and experience with SDTM/ADaM/Define.xml.
• Experience supporting regulatory submissions and FDA/ICH interactions.

Responsabilidades

• Generate SDTM/ADaM specifications, datasets, reviewer's guides, and define.xmls for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality SAS/R outputs for clinical development programs and CRO oversight.
• Support clinical study reports, regulatory submissions, DSURs, and exploratory analyses.
• Collaborate with CROs and vendors to meet timelines and quality standards.
• Review SOPs and create data transfer specifications as needed.

Conocimientos

SAS programming

R programming

CDISC SDTM/ADaM/Define.xml

Regulatory submissions support

Independent work

Communication & leadership

Educación

Bachelor's degree in CS/Data Science/Math/Statistics

Herramientas

SAS

R

Python

Java

Shiny

Unix/Linux

Git

Descripción del empleo

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely on sponsor-dedicated projects with global pharmaceutical clients.

You will implement reporting and analysis activities, oversee CRO programmers, and ensure high-quality data outputs while adhering to FDA/ICH regulations. The role requires independent work, extensive SDTM/ADaM experience, and strong communication and leadership skills.