Senior Statistical Programmer (SAS + R) – Remote

Leader Clinics

Málaga

Remote

EUR 60,000 - 90,000

Full time

5 days ago

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Job summary

Cytel is seeking a Senior Statistical Programmer SAS + R to join one of our global pharmaceutical clients. This fully remote role focuses on advanced SAS programming and CDISC SDTM/ADaM standards to support multiple Phase I–IV trials and deliver high-quality analysis datasets and reports.

You will lead data manipulation, analysis, TLF generation, submission documents, and collaborate with cross-functional teams.

Qualifications

Bachelor's degree in Statistics, Computer Science, or Mathematics.
8+ years SAS programming with clinical trial data in the Pharmaceutical/Biotech industry; master’s degree or higher preferred.
Strong SAS data manipulation, analysis and reporting skills.
Solid experience implementing the latest CDISC SDTM/ADaM standards.
Experience with submissions documentation (define.xml) is a plus.

Responsibilities

Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy).
Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
Production and QC / validation programming.
Generating complex ad-hoc reports utilizing raw data.
Applying strong understanding/experience of Efficacy analysis.
Creating and reviewing submission documents and eCRTs.
Communicating with cross-functional teams and clients on project specs and status.
Performing lead duties when called upon.