Remote Lead Statistical Programmer (SAS, CDISC)

Kyverna Therapeutics

United States

Remote

USD 166.000 - 208.000

Vollzeit

Vor 8 Tagen

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Zusammenfassung

Kyverna Therapeutics is seeking a Statistical Programmer Consultant to independently lead programming activities for designated clinical trials, developing SDTM/ADaM datasets and regulatory deliverables.

This remote role (West Coast hours preferred) offers a 6-month duration, 40 hours per week, and an hourly rate of $80–$100, with strong emphasis on CDISC standards, SAS programming, and cross-functional collaboration.

Qualifikationen

  • Bachelor’s or Master’s degree in statistics, biostatistics, CS, math or related field.
  • 8+ years of statistical programming experience in biopharma or CRO.
  • Advanced proficiency in SAS including data steps, macros, and PROCs.
  • Strong CDISC standards knowledge; experience with define.xml and ADRG/cSDRG.
  • Excellent communication and ability to manage multiple projects remotely.

Aufgaben

  • Lead programming for assigned trials and collaborate with statisticians and data management.
  • Design, map, and validate SDTM/ADaM datasets with data traceability.
  • Perform TLFs using SAS to support CSRs, DSURs, ad-hoc reports, and submissions.
  • Ensure CDISC packages meet regulatory requirements and submission standards.
  • Perform additional duties as assigned.

Kenntnisse

SAS programming
CDISC (SDTM/ADaM)
Clinical trial data analysis
Regulatory submission artifacts

Ausbildung

Statistics/Biostatistics degree

Tools

Pinnacle 21
SAS Macro Language

Jobbeschreibung

Kyverna Therapeutics is seeking a Statistical Programmer Consultant to independently lead programming activities for designated clinical trials, developing SDTM/ADaM datasets and regulatory deliverables.

This remote role (West Coast hours preferred) offers a 6-month duration, 40 hours per week, and an hourly rate of $80–$100, with strong emphasis on CDISC standards, SAS programming, and cross-functional collaboration.

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