Senior Statistical Programmer – Remote (SAS + CDISC)

Welocalize, Inc

Zaragoza

Remote

EUR 107,000 - 142,000

Full time

2 days ago
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Benefits offered by this job

Remote work

Job summary

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to support one or more global pharmaceutical trials. You will leverage advanced SAS programming and CDISC SDTM/ADaM standards to develop analysis datasets, tables, listings, and figures, with opportunities to lead projects.

This fully remote role suits candidates with strong data manipulation, efficacy analysis experience, and a proven ability to deliver high-quality outputs on tight timelines.

Qualifications

  • 8+ years SAS programming experience with clinical trial data in Pharma/Biotech; bachelor’s degree or equivalent; 6+ years with a master’s degree or above.
  • Study lead experience, juggling multiple projects is preferred.
  • Strong SAS data manipulation, analysis and reporting skills.
  • Solid experience implementing CDISC SDTM/ADaM standards.
  • Strong QC/validation skills and good ad-hoc reporting.
  • Proficiency in efficacy analysis and submissions (define.xml).
  • Experience supporting immunology, respiratory or oncology studies is a plus.
  • Excellent analytical and troubleshooting skills; able to meet tight timelines with global teams.

Responsibilities

  • Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy) using SAS.
  • Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
  • Production and QC / validation programming.
  • Generate complex ad-hoc reports from raw data.
  • Apply strong understanding of efficacy analysis.
  • Create and review submission documents and define.xml.
  • Communicate with internal cross-functional teams and client for project specs and status.
  • Perform lead duties when called upon.
  • Be a team player and adapt to changing priorities.

Skills

SAS programming
CDISC SDTM/ADaM
Data analysis
Data manipulation
Ad-hoc reporting
QC/validation
Efficacy analysis
Leadership
Cross-functional teamwork
Communication

Education

Bachelor's degree in Statistics, Computer Science, Mathematics
Master's degree or above preferred

Tools

R programming

Job description

Cytel Inc. is seeking a Senior/Principal Statistical Programmer to support one or more global pharmaceutical trials. You will leverage advanced SAS programming and CDISC SDTM/ADaM standards to develop analysis datasets, tables, listings, and figures, with opportunities to lead projects.

This fully remote role suits candidates with strong data manipulation, efficacy analysis experience, and a proven ability to deliver high-quality outputs on tight timelines.

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