Senior Principal Statistical Programmer (SAS + R) - Remote

Colegio Oficial De Farmacéuticos De Cádiz; Cádiz; Remoto; EUR 89.000 - 134.000; Tempo pieno

Descrizione del lavoro

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-dedicated program. You will work on clinical development programs across therapeutic areas, implementing reporting and analysis activities for sponsor trials.

The role requires strong SAS/R skills, CDISC SDTM/ADaM expertise, and experience with regulatory submissions. You will lead CRO programming deliverables and collaborate with internal and external partners to ensure high-quality results.

Competenze

• Bachelor's degree in computer science, data science, mathematics, or statistics.
• 7+ years as Statistical Programmer in Biotech/Pharma Biostatistics team or similar.
• Exceptional SAS programming skills and SDTM/ADaM/Define.xml experience.
• Experience with regulatory submissions and FDA/ICH guidelines.
• Ability to work independently and lead CRO programming deliverables.

Mansioni

• Generate SDTM/ADaM specifications, datasets, reviewer's guides, and define.xml for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs.
• Deliver high-quality SAS/R outputs and oversee CRO programmers to meet timelines.
• Support preparation of CSRs, regulatory submissions, publications, and DSURs.
• Collaborate with CROs, vendors, and clinical development partners to ensure project milestones.

Conoscenze

SAS programming

R programming

CDISC standards

Leadership

Communication

Formazione

Bachelor's degree in CS/DS/Math/Statistics

Strumenti

SAS

R

Python

Shiny

Unix/Linux

Git

Descrizione del lavoro

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (Remote) to join a sponsor-dedicated program. You will work on clinical development programs across therapeutic areas, implementing reporting and analysis activities for sponsor trials.

The role requires strong SAS/R skills, CDISC SDTM/ADaM expertise, and experience with regulatory submissions. You will lead CRO programming deliverables and collaborate with internal and external partners to ensure high-quality results.