Senior Statistical Programmer (SAS + R) Remote

N-Ix; Granada; Remote; EUR 80,000 - 111,000; Full time

Job summary

Cytel Inc. is recruiting a Senior/Principal Statistical Programmer (SAS + R) for a fully remote role. You will be embedded with a pharmaceutical client, handling advanced SAS programming, SDTM/ADaM data creation and submission documentation, across multiple phases of clinical trials.

The role emphasizes data manipulation, analysis and reporting, with opportunities to lead teams, respond to client inquiries, and adapt to changing priorities in a globally distributed environment.

Qualifications

• Bachelor's degree in Statistics, Computer Science, Mathematics, or related field.
• 7+ years SAS programming with clinical trial data; 6+ years with Master's degree or above.
• Strong SAS data manipulation, analysis and reporting skills.
• Experience implementing CDISC SDTM/ADaM standards.
• Proficient in creating and validating submission-ready datasets and TLFs.
• Excellent analytical and troubleshooting abilities.
• Experience with epilepsy studies is a plus.

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy).
• Generate and validate SDTM/ADaM datasets and tables, listings and figures (TLFs).
• Handle production and QC/validation programming.
• Create complex ad-hoc reports from raw data.
• Apply strong efficacy analysis expertise.
• Prepare submission documents and eCRTs.
• Communicate with cross-functional teams and clients on project specs and issues.
• Lead duties when required.
• Collaborate effectively in a globally dispersed team.

Skills

SAS programming

CDISC SDTM/ADaM

Clinical data analysis

Ad-hoc reporting

QC/validation

Efficacy analysis

Submission documents

Leadership duties

Team communication

Education

Bachelor's degree

Master's degree

Tools

SAS software

Job description

Cytel Inc. is recruiting a Senior/Principal Statistical Programmer (SAS + R) for a fully remote role. You will be embedded with a pharmaceutical client, handling advanced SAS programming, SDTM/ADaM data creation and submission documentation, across multiple phases of clinical trials.

The role emphasizes data manipulation, analysis and reporting, with opportunities to lead teams, respond to client inquiries, and adapt to changing priorities in a globally distributed environment.