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Hiring companyCytel

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Senior Statistical Programmer FSP

India Full-time Remote

About the role

Statistical Programming team at Cytel supports pharmaceutical clients by developing SAS programs and CDISC SDTM/ADaM datasets for clinical trials. The Senior Statistical Programmer leverages advanced SAS skills to design, validate, and deliver data sets, analysis files, and submission documents, while leading project tasks and collaborating with global cross-functional teams. Remote, India.

What you’ll do

  • Perform data manipulation, analysis and reporting of clinical trial safety and efficacy data using SAS
  • Generate and validate SDTM and ADaM datasets, analysis files, and TLFs
  • Conduct production and QC/validation programming
  • Create complex ad‑hoc reports from raw data
  • Apply expertise in efficacy analysis
  • Prepare and review submission documents and eCRTs
  • Communicate with cross‑functional teams and clients on project specifications and status
  • Lead duties when required

What you’ll bring

  • Bachelor’s degree in Statistics, Computer Science, Mathematics or related field
  • At least 8 years SAS programming experience in pharma/biotech clinical trials
  • Strong SAS data manipulation, analysis and reporting skills
  • Solid experience with CDISC SDTM & ADaM standards
  • Strong QC/validation skills
  • Proficiency in efficacy analysis
  • Experience with define.xml and submission documents
  • Experience supporting immunology, respiratory or oncology studies (plus)

Nice to have

  • Bachelor’s degree in Statistics, Computer Science, Mathematics or related field
  • 8+ years SAS programming in clinical trials
  • 6+ years related experience with master’s degree or above

Skills

SAS programmingCDISC SDTMADaMClinical trialsData validationEfficacy analysisSubmission documentsQC