Senior Principal Statistical Programmer (SAS & R) – Remote

Moniepoint Inc.

Huelva

À distance

EUR 70 000 - 110 000

Plein temps

Il y a 5 jours
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Résumé du poste

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to be fully embedded with one global pharmaceutical client. You will implement reporting and analysis activities for sponsor clinical trials, ensuring data quality and regulatory compliance.

As a principal programmer you will lead SDTM/ADaM workstreams, supervise CROs, and contribute to study reports and regulatory submissions in a remote, sponsor-dedicated environment.

Qualifications

  • Extensive experience in clinical trial data analysis and reporting.
  • Proven ability to develop SDTM/ADaM datasets and specifications.
  • Experience overseeing CRO programmers to ensure timely, high-quality deliverables.

Responsabilités

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

Connaissances

SAS programming
R programming
SDTM/ADaM
Clinical data standards
Regulatory knowledge
CRO oversight

Formation

Advanced degree in Biostatistics/Statistics or related field

Outils

SAS Software
R

Description du poste

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to be fully embedded with one global pharmaceutical client. You will implement reporting and analysis activities for sponsor clinical trials, ensuring data quality and regulatory compliance.

As a principal programmer you will lead SDTM/ADaM workstreams, supervise CROs, and contribute to study reports and regulatory submissions in a remote, sponsor-dedicated environment.

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