Senior Statistical Programmer Consultant (Oncology)

TL;DR

Senior Statistical Programmer Consultant (Oncology): Leading end-to-end programming deliverables for oncology clinical trials with an accent on CDISC standards, SDTM/ADaM dataset development, and regulatory submissions. Focus on providing technical leadership, managing study timelines, and ensuring high-quality programming outputs for FDA/EMA/PMDA compliance.

Location: Must be based in the United States

Company

hirify.global is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies.

What you will do

• Lead programming activities for oncology clinical trials across multiple studies.
• Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
• Oversee the production of Tables, Listings, and Figures (TLFs) for study reporting and submissions.
• Provide SAS programming expertise to support complex data derivations and analyses.
• Coordinate with CROs and external vendors to ensure compliance and quality.
• Support integrated analyses including ISS/ISE and prepare submission-ready documentation.

Requirements

• Must be based in the United States
• Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, or Life Sciences.
• 8–12+ years of statistical programming experience in pharma, biotech, or CRO.
• Expert-level proficiency in SAS.
• Strong understanding of CDISC SDTM and ADaM standards.
• Significant experience supporting oncology clinical trials and regulatory submissions.

Culture & Benefits

• Opportunity to work directly for a single sponsor while maintaining the security of a global CRO.
• Commitment to continuous training and professional development.
• Focus on diversity, inclusivity, and employee well-being.
• Below industry average turnover rates.

Hiring process

• Initial CV review and acknowledgement.
• Phone interview for qualified candidates.