Senior Statistical Programmer - Remote SDTM/ADaM Lead

Cytel; España; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Cytel is seeking a Senior Statistical Programmer to join a fully remote role embedded with a pharmaceutical client. You will leverage SAS programming and CDISC SDTM/ADaM standards to support Phase I-IV trials, with autonomy and ownership over deliverables.

You will collaborate with global teams to produce data listings, tables, and figures, perform validation, and contribute to submissions. Strong analytical skills and clinical trial data experience are essential.

Formación

• Bachelor’s degree in Statistics, Computer Science, or Mathematics.
• 8+ years SAS programming experience with clinical trial data.
• Strong knowledge of CDISC SDTM/ADaM standards.
• Experience leading multiple projects and cross-functional teams.
• Excellent analytical and troubleshooting skills.

Responsabilidades

• Perform data manipulation, analysis and reporting of trial data.
• Generate and validate SDTM/ADaM datasets and TLFs.
• Production and QC / validation programming.
• Generate complex ad-hoc reports from raw data.
• Applying strong understanding/experience of Efficacy analysis.
• Creating and reviewing submission documents and eCRTs.
• Communicating with internal cross-functional teams and client for project specifications, status, issues or inquiries.
• Performing lead duties when called upon.
• Serving as a team player and meeting deadlines.

Conocimientos

SAS programming

CDISC SDTM/ADaM

Data manipulation

Clinical trial data

Ad-hoc reporting

Leadership

Educación

Bachelor’s degree in Statistics/Computer Science/Math

Master’s degree in related field

Herramientas

SAS

CDISC tools

Descripción del empleo

Cytel is seeking a Senior Statistical Programmer to join a fully remote role embedded with a pharmaceutical client. You will leverage SAS programming and CDISC SDTM/ADaM standards to support Phase I-IV trials, with autonomy and ownership over deliverables.

You will collaborate with global teams to produce data listings, tables, and figures, perform validation, and contribute to submissions. Strong analytical skills and clinical trial data experience are essential.