Senior Statistical Programmer (SAS + R) Remote

Act Digital Emea - Alter Solutions; Málaga; Remote; EUR 60,000 - 90,000; Full time

Job summary

Cytel Inc. is seeking a Senior Statistical Programmer to drive SAS programming for clinical trials in a fully remote role. You will manipulate data, develop SDTM/ADaM datasets and analysis files, and prepare tables, listings and figures (TLFs) for submissions.

The ideal candidate brings 8+ years of SAS experience in pharma/biotech, strong CDISC expertise, and the ability to lead studies and collaborate with global cross-functional teams.

Qualifications

• 8+ years SAS programming on clinical trial data in pharma/biotech.
• Solid experience implementing CDISC SDTM/ADaM standards.
• Strong QC/validation and data analysis skills.
• Experience leading studies and coordinating cross-functional teams.

Responsibilities

• Manipulate, analyze and report clinical trial data (safety and efficacy).
• Create SDTM/ADaM datasets and analysis files and TLFs.
• Produce and QC/validate programming outputs.
• Generate complex ad-hoc reports from raw data.
• Apply expertise in efficacy analyses for submissions.

Skills

SAS programming

CDISC SDTM/ADaM

Data manipulation

Ad-hoc reporting

Study lead

Education

BSc Statistics

MSc or higher

Job description

Cytel Inc. is seeking a Senior Statistical Programmer to drive SAS programming for clinical trials in a fully remote role. You will manipulate data, develop SDTM/ADaM datasets and analysis files, and prepare tables, listings and figures (TLFs) for submissions.

The ideal candidate brings 8+ years of SAS experience in pharma/biotech, strong CDISC expertise, and the ability to lead studies and collaborate with global cross-functional teams.