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Principal Statistical Programmer Consultant

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Location: Remote
Compensation: To Be Discussed
Reviewed: Fri, Nov 06, 2026
This job expires in: 30 days

Job Summary

To support clinical development programs in solid tumor oncology, the full-time remote Principal Statistical Programmer Consultant will lead statistical programming activities, develop and validate datasets, and ensure compliance with CDISC standards while collaborating with cross-functional teams.

Key Responsibilities
  • Lead and oversee statistical programming activities for oncology clinical trials, focusing on solid tumor indications
  • Develop, validate, and maintain SDTM and ADaM datasets in compliance with CDISC standards
  • Program and review complex TFLs for clinical study reports and regulatory submissions
Required Qualifications
  • Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related discipline
  • Extensive experience in clinical statistical programming within the pharmaceutical or biotechnology industry
  • Strong hands-on experience with SAS programming, including SAS Base, SAS Macro, and SAS/STAT
  • Significant experience supporting solid tumor oncology clinical trials across Phase I, II, and III studies
  • Expertise in CDISC SDTM and ADaM standards

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