Senior Statistical Programmer (SAS/R) – Remote/CDISC SDTM/ADaM

The Door Talent

Madrid

Remote

EUR 70,000 - 130,000

Full time

4 days ago
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Job summary

Cytel, a leading partner in pharmaceutical data science, seeks a Senior/Principal Statistical Programmer to support one global client from a remote setup. You will apply advanced SAS programming and CDISC SDTM/ADaM expertise to Phase I–IV trials, delivering analyses, datasets, tables, listings and figures.

You will contribute as a senior team member, lead when required, collaborate with cross-functional groups, ensure quality submissions, and adapt to changing priorities while maintaining

Qualifications

  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 8 years of SAS programming with clinical trial data in Pharma/Biotech; master's degree or above for 6+ years of related experience.
  • Study lead experience preferred; ability to juggle multiple projects.

Responsibilities

  • Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy) using SAS.
  • Generate and validate SDTM and ADaM datasets/files, tables, listings, and figures (TLFs).
  • Produce and QC/validate programming outputs.
  • Create complex ad-hoc reports from raw data.
  • Apply strong efficacy analysis understanding.
  • Assist in submissions documents and eCRTs.
  • Communicate with cross-functional teams and clients on specifications and status.
  • Take on lead duties when required.

Skills

SAS programming
CDISC SDTM/ADaM
Data manipulation
Analysis and reporting
Lead duties

Education

Bachelor's degree in Statistics/Computer Science/Mathematics
Master's degree or higher preferred

Tools

SAS Software

Job description

Cytel, a leading partner in pharmaceutical data science, seeks a Senior/Principal Statistical Programmer to support one global client from a remote setup. You will apply advanced SAS programming and CDISC SDTM/ADaM expertise to Phase I–IV trials, delivering analyses, datasets, tables, listings and figures.

You will contribute as a senior team member, lead when required, collaborate with cross-functional groups, ensure quality submissions, and adapt to changing priorities while maintaining

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