Senior Statistical Programmer (SAS + R) – Remote

Thedoortalent

La Coruña

Remote

EUR 70,000 - 110,000

Full time

8 days ago

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Job summary

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely within our sponsor-dedicated model in Spain. You will lead complex programming tasks across SDTM/ADaM, define.xml, and CSR support, while coordinating with CROs to ensure timely, high-quality deliverables.

The role requires extensive SAS expertise, CDISC standards, and experience with regulatory submissions. Strong communication and independent working style are essential in this client-focused setting.

Qualifications

  • Bachelor's degree in a relevant field; strong statistics background preferred.
  • 7+ years as Statistical Programmer in Biotech/Pharma clinical development.
  • Expert SAS programming with CDISC SDTM/ADaM/Define.xml experience.
  • Experience supporting regulatory submissions and interactions with authorities.
  • Ability to work independently with strong communication and leadership.

Responsibilities

  • Generate SDTM, ADaM specs, datasets, and define.xml across studies.
  • Develop SAS programs for datasets, listings, tables and graphs.
  • Deliver high-quality SAS/R outputs for clinical development programs.
  • Oversee CRO programming deliverables to meet timelines.
  • Support preparation of CSRs, regulatory submissions, DSURs and analyses.
  • Adhere to FDA/ICH guidance and good clinical practice standards.
  • Contribute to programming standards, CRFs, edit checks, and data validation plans.

Skills

SAS programming
CDISC standards
Regulatory submissions
Independent worker
Communication skills

Education

Bachelor's degree in Computer Science/Data Science/Math/Statistics

Tools

R
Python
Java
Shiny
Markdown
Unix/Linux
Git

Job description

Cytel is seeking a Senior/Principal Statistical Programmer (SAS + R) to work remotely within our sponsor-dedicated model in Spain. You will lead complex programming tasks across SDTM/ADaM, define.xml, and CSR support, while coordinating with CROs to ensure timely, high-quality deliverables.

The role requires extensive SAS expertise, CDISC standards, and experience with regulatory submissions. Strong communication and independent working style are essential in this client-focused setting.

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