Senior Principal Statistical Programmer (SAS & R) - Remote

Standard Bank Group

Cape Town

A distancia

ZAR 1.000.000 - 1.300.000

Jornada completa

Hace 5 días
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Descripción de la vacante

Cytel is seeking a Senior/Principal Statistical Programmer SAS + R for remote embedding with a pharma client. You will join a sponsor-dedicated team to drive high-quality analytical outputs and regulatory-ready deliverables.

You will implement SDTM/ADaM specs, develop complex SAS/R programs, and oversee CRO programming across studies. Regulatory submissions and data reviews are integral to the role.

Formación

  • Senior/Principal Statistical Programmer with SAS and R experience.
  • Experience implementing SDTM/ADaM specifications and data listings.
  • Ability to oversee CRO programmers and ensure high-quality outputs.

Responsabilidades

  • Generate SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies
  • Develop SAS programs to generate datasets, listings, tables and graphs
  • Deliver high-quality statistical programming results including SAS and/or R programs
  • Oversee CRO programming deliverables to meet timelines
  • Support preparation of clinical study reports, regulatory submissions, publications, and DSUR
  • Follow FDA regulations and guidelines for electronic submissions
  • Contribute to standards for programming tools and macros
  • Develop CRFs, edit check specs, and data validation plans
  • Review and/or author data as needed

Conocimientos

SAS programming
R programming
SDTM/ADaM standards
Clinical programming leadership
CRO oversight
Regulatory submissions
FDA guidelines
Data analysis

Herramientas

SAS
R

Descripción del empleo

Cytel is seeking a Senior/Principal Statistical Programmer SAS + R for remote embedding with a pharma client. You will join a sponsor-dedicated team to drive high-quality analytical outputs and regulatory-ready deliverables.

You will implement SDTM/ADaM specs, develop complex SAS/R programs, and oversee CRO programming across studies. Regulatory submissions and data reviews are integral to the role.

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