Senior Statistical Programmer (SAS/R) – Remote

Dentaid; País Vasco; Remote; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Remote work

Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join our sponsor-dedicated, embedded team supporting global pharmaceutical clients. You will independently manage programming deliverables, develop SAS/R pipelines, and oversee CROs to ensure high-quality data outputs for submissions.

You will work on SDTM/ADaM specifications, create complex listings and graphs, and contribute to study reports and regulatory submissions while following FDA/ICH guidelines.

Qualifications

• Advanced SAS programming experience in clinical trials.
• Experience with SDTM/ADaM data structures and specs.
• Strong track record delivering high-quality programming outputs for regulatory submissions.

Responsibilities

• Generate SDTM, ADaM specifications, datasets, reviewer’s guides and define.xml files for multiple studies.
• Develop SAS programs to create datasets, listings, tables, and graphs with descriptive and inferential stats.
• Deliver high-quality programming results and maintain SAS and R programs for clinical programs.
• Oversee CRO programmers to ensure timely, high-quality deliverables for multiple studies.
• Support preparation of clinical study reports, regulatory submissions, and exploratory analyses.
• Ensure adherence to FDA regulations and good clinical practice for electronic submissions.
• Contribute to standards for programming tools, outputs, and macros.

Skills

SAS

R

SDTM/ADaM specs

Clinical programming

CRO oversight

Regulatory submissions

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to join our sponsor-dedicated, embedded team supporting global pharmaceutical clients. You will independently manage programming deliverables, develop SAS/R pipelines, and oversee CROs to ensure high-quality data outputs for submissions.

You will work on SDTM/ADaM specifications, create complex listings and graphs, and contribute to study reports and regulatory submissions while following FDA/ICH guidelines.