Principal Statistical Programmer (SAS + R) - Remote

Placements24

Polokwane

Remoto

ZAR 2.160.000 - 2.991.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Descrizione del lavoro

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to join our sponsor-dedicated team embedded with a pharmaceutical client. You will work independently with expert support, leading programming efforts across multiple studies and overseeing CRO deliverables.

The role emphasizes SAS programming excellence, CDISC standards (SDTM/ADaM/Define.xml), regulatory submissions readiness, and collaboration with cross-functional partners to ensure timely, high-quality data outputs.

Competenze

  • 7+ years of experience as a Statistical Programmer on Biotech/Pharma clinical development biometrics teams or similar.
  • Exceptional SAS programming skills and experience in clinical development environments.
  • Extensive applied experience with CDISC standards (SDTM, ADaM, Define.xml) and regulatory guidelines.
  • Experience supporting regulatory submissions and interactions with FDA/global authorities.

Mansioni

  • Generate SDTM/ADaM specifications, datasets, revieweras guides and define.xml files for multiple studies.
  • Develop SAS programs to produce datasets, listings, tables, and graphs.
  • Deliver high-quality statistical programming outputs and maintain SAS and/or R programs.
  • Oversee CRO programming deliverables to meet timelines and quality standards.
  • Support preparation of clinical study reports, regulatory submissions, publications, and DSURs.

Conoscenze

SAS programming
Leadership
Communication (written & verbal)

Formazione

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

Strumenti

R
Python
Unix/Linux
git

Descrizione del lavoro

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to join our sponsor-dedicated team embedded with a pharmaceutical client. You will work independently with expert support, leading programming efforts across multiple studies and overseeing CRO deliverables.

The role emphasizes SAS programming excellence, CDISC standards (SDTM/ADaM/Define.xml), regulatory submissions readiness, and collaboration with cross-functional partners to ensure timely, high-quality data outputs.

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