Senior/Principal Statistician Consultant (Oncology)

Location: Remote within the United States; availability required during core U.S. business hours, generally 9:00 a.m.–3:00 p.m. Eastern Time.

Company

hirify.global is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

What you will do

• Support statistical analyses of oncology endpoints, including time-to-event and response-based endpoints.
• Perform event projections to estimate the timing of planned event-driven analyses.
• Review SDTM and ADaM specifications, tables, listings, figures, statistical analysis plans, protocol amendments, and related study documentation.
• Conduct routine study data reviews to identify inconsistencies, missing data, unexpected patterns, and other issues affecting analysis or interpretation.
• Validate statistical outputs and document findings to support reproducibility and quality control.
• Collaborate with study teams, programming teams, and functional partners to resolve data and analysis questions.

Requirements

• Experience supporting Phase 2 and Phase 3 oncology clinical trials, including event-driven and response-based endpoints.
• Experience reviewing clinical trial data, documenting findings and assumptions, raising queries, and tracking issues through resolution.
• Working knowledge of CDISC standards, including SDTM and ADaM.
• Strong analytical, written communication, and statistical analysis skills, with a methodical approach to issue identification.
• Proficiency with statistical programming and data processing software such as SAS and/or R.
• PhD or equivalent degree in statistics, biostatistics, or a related discipline with at least 3 years of relevant experience, or a Master’s degree with at least 6 years of relevant experience.

Culture & Benefits

• Work with a diverse client portfolio across pharmaceutical, biotechnology, medical device, and consumer health sectors.
• Collaborate with U.S.-based study teams and international functional partners.
• Access to continuous training and professional development focused on maintaining high-quality expertise.
• Work within a quality-driven one-team culture centered on healthcare and clinical development.

Hiring process

• Submit a CV and receive an application acknowledgement.
• Qualified candidates are invited to a phone interview as the first step.