Senior Statistical Programmer - Remote (SAS, CDISC)

Cytel; Abla; A distancia; EUR 97.000 - 141.000; Jornada completa

Descripción de la vacante

Cytel is seeking a Senior Statistical Programmer to work with one of our global pharmaceutical clients. You will leverage advanced SAS programming and CDISC SDTM/ADaM standards to support Phase I–IV trials, with the role offered as fully remote.

You will lead data manipulation, analysis and reporting, generate and validate datasets, create TLFs, and contribute to submission documents while collaborating with cross‑functional teams worldwide and meeting stringent timelines.

Formación

• Bachelor’s degree in Statistics, Computer Science, Mathematics, etc.
• 7+ years SAS programming with clinical trial data.
• Strong SDTM/ADaM CDISC standards experience.
• Experience with epilepsy studies is a plus.

Responsabilidades

• Perform data manipulation, analysis and reporting of clinical trial data using SAS.
• Generate and validate SDTM/ADaM datasets/analysis files and TLFs.
• Production and QC/validation programming.
• Generate complex ad-hoc reports from raw data.
• Apply expertise in efficacy analysis.
• Create and review submission documents including define.xml.
• Collaborate with cross-functional teams and clients on project specs and status.
• Provide lead duties when required.
• Be adaptable to changing priorities and deadlines.

Conocimientos

SAS programming

CDISC SDTM/ADaM

Data manipulation

Ad-hoc reporting

Efficacy analysis

Clinical trial data familiarity

Cross-functional communication

Educación

Bachelor’s degree in Statistics, Computer Science, Mathematics, etc.

Master’s degree or higher (preferred)

Descripción del empleo

Cytel is seeking a Senior Statistical Programmer to work with one of our global pharmaceutical clients. You will leverage advanced SAS programming and CDISC SDTM/ADaM standards to support Phase I–IV trials, with the role offered as fully remote.

You will lead data manipulation, analysis and reporting, generate and validate datasets, create TLFs, and contribute to submission documents while collaborating with cross‑functional teams worldwide and meeting stringent timelines.