Senior Principal Statistical Programmer (SAS + R) — Remote

Vitaldent

Badajoz

Remote

EUR 70,000 - 100,000

Full time

14 days+

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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to work on pharmaceutical client programs, delivering high-quality SAS and R programming, SDTM/ADaM specs, and DEFINE.XML.

You will lead programming deliverables, oversee CROs, contribute to study reports and regulatory submissions, and ensure compliance with FDA guidelines and CDISC standards.

Join a collaborative team that values autonomy and ownership in a fully embedded sponsor environment.

Qualifications

  • Bachelor level degree in a related field or equivalent experience.
  • 7+ years of experience as a Statistical Programmer in Biotech/Pharma.
  • Strong SAS programming skills and CDISC SDTM/ADaM Define.xml experience.

Responsibilities

  • Generate SDTM and ADaM specifications, datasets, and define.xmls for multiple studies.
  • Develop SAS programs to produce datasets, listings, tables and graphs.
  • Deliver high-quality SAS/R outputs for clinical development programs.
  • Oversee CRO programming deliverables to meet timelines and quality standards.
  • Support clinical study reports, regulatory submissions, and publications.
  • Adhere to FDA regulations, GCP, and eSubmissions guidelines.
  • Contribute to standards for programming tools, outputs, and macros.
  • Assist in CRF development, edit checks, and data validation plans.
  • Provide review/author data transfer specifications for external data.

Skills

SAS programming
CDISC standards
Clinical data analysis
CRO oversight

Education

Bachelor's degree in computer science/data science/mathematics/statistics

Tools

R
SAS

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (Remote) to work on pharmaceutical client programs, delivering high-quality SAS and R programming, SDTM/ADaM specs, and DEFINE.XML.

You will lead programming deliverables, oversee CROs, contribute to study reports and regulatory submissions, and ensure compliance with FDA guidelines and CDISC standards.

Join a collaborative team that values autonomy and ownership in a fully embedded sponsor environment.

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