Remote Principal Statistical Programmer (SAS + R)

Jobgether Srl; Málaga; Remote; EUR 90.000 - 130.000; Vollzeit

Zusammenfassung

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to be fully remote and dedicated to a pharmaceutical client.

You will lead programming activities, generate SDTM/ADaM specifications, create tables, listings, and graphs, and oversee CROs to ensure timely, high-quality outputs. The role demands strong SAS and CDISC expertise, regulatory submission experience, and independent, proactive collaboration with cross-functional teams.

Qualifikationen

• Bachelor’s degree in computer science, data science, mathematics or statistics.
• 7+ years of experience as a Statistical Programmer in Biotech/Pharma.
• Exceptional SAS programming skills and experience with SDTM/ADaM and Define.xml.
• Experience supporting regulatory submissions and interactions with regulators.
• Ability to work independently and lead cross-functional collaboration.
• Strong written and verbal communication and leadership abilities.

Aufgaben

• Generate SDTM, ADaM specifications, datasets, reviewer's guides and define.xml files.
• Develop SAS programs to create datasets, listings, tables and graphs.
• Deliver high-quality programming outputs for regulatory submissions.
• Oversee CRO programming deliverables across multiple studies and timelines.
• Contribute to clinical study reports and exploratory analyses.
• Develop and maintain standards for programming tools, outputs and macros.

Kenntnisse

SAS programming

CDISC SDTM/ADaM/Define.xml

Regulatory submissions experience

Independent work

Communication skills

Leadership skills

R

Python

Unix/Linux

Git

Ausbildung

Bachelor's degree in Computer Science, Data Science, Mathematics, or Statistics

Tools

SAS

R

Python

Java

Shiny

Markdown

Unix/Linux

Git

Jobbeschreibung

Cytel Inc. is seeking a Senior/Principal Statistical Programmer (SAS + R) to be fully remote and dedicated to a pharmaceutical client.

You will lead programming activities, generate SDTM/ADaM specifications, create tables, listings, and graphs, and oversee CROs to ensure timely, high-quality outputs. The role demands strong SAS and CDISC expertise, regulatory submission experience, and independent, proactive collaboration with cross-functional teams.