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Responsibilities:
- Act as lead programmer for assigned clinical trials, providing expert statistical programming support.
- Guide the design, mapping, and validation of SDTM and ADaM datasets with full traceability.
- Generate and validate Tables, Listings, and Figures (TLFs) using SAS for CSRs, DSURs, and ad-hoc requests.
Qualifications:
- Bachelor's or Master's in Statistics, Biostatistics, Computer Science, or related scientific discipline.
- 8+ years of statistical programming experience in biopharma or CRO.
- Advanced SAS proficiency and comprehensive understanding of CDISC standards and eCTD submissions.
Work Environment:
- Remote role with West coast hours preferred.
- 6-month contract at $80-100 per hour.
- Collaborative, fast-paced, cross-functional team culture.
Kyverna Therapeutics
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company developing cell therapies for patients suffering from autoimmune diseases. Guided by core values of collaboration and innovation, the company is committed to transforming the future of treatment for autoimmune disease.