Principal Statistical Programmer (SAS & R) - Remote

Reformas Rapido Sl

Allande

Remote

EUR 107,000 - 134,000

Full time

4 days ago
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Job summary

Cytel invites applications for a Senior/Principal Statistical Programmer (Remote). You will work embedded with a pharmaceutical client, delivering end-to-end programming for clinical trials. The role emphasizes independence, regulatory compliance, and collaboration with CROs to ensure high-quality data outputs.

You will develop SDTM/ADaM specifications, write SAS/R code for analyses and tables, and contribute to study reports and regulatory submissions in a fast-paced setting.

Qualifications

  • Experience in clinical development programming across multiple therapeutic areas.
  • Proven ability to implement SDTM/ADaM specifications and create CRFs/edit checks.
  • Experience overseeing CROs and delivering high-quality programming outputs on time.

Responsibilities

  • Generate SDTM/ADaM specifications, datasets, reviewer’s guides and define.xml files for studies.
  • Develop SAS programs to produce datasets, listings, tables and complex graphs.
  • Deliver high-quality programming outputs and maintain SAS/R programs for clinical development programs.
  • Oversee CRO programmers to ensure timely, accurate deliverables.

Skills

SAS programming
R programming
SDTM
ADaM
CRO oversight
Regulatory submissions
FDA guidelines
GCP

Tools

define.xml

Job description

Cytel invites applications for a Senior/Principal Statistical Programmer (Remote). You will work embedded with a pharmaceutical client, delivering end-to-end programming for clinical trials. The role emphasizes independence, regulatory compliance, and collaboration with CROs to ensure high-quality data outputs.

You will develop SDTM/ADaM specifications, write SAS/R code for analyses and tables, and contribute to study reports and regulatory submissions in a fast-paced setting.

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