Biostatistician (Clinical Research)

TL;DR

Biostatistician (SAS/R): Analyzing and validating clinical trial data to ensure compliance with regulatory standards with an accent on TFL production and SAP interpretation. Focus on performing survival analysis, mixed models, and preparing regulatory submission data.

Location: Remote

Salary: $60–$65/hour

Company

hirify.global provides specialized consulting services for clinical research projects.

What you will do

• Analyze and validate clinical trial data.
• Review and interpret Statistical Analysis Plans (SAPs).
• Produce and quality-check Tables, Figures & Listings (TFLs).
• Review Clinical Study Reports (CSRs) and regulatory submission data.
• Perform statistical analyses using SAS and/or R.
• Collaborate with cross-functional teams and document findings accurately.

Requirements

• 5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research).
• MSc or PhD in Biostatistics, Statistics, or a related field.
• Proficiency in SAS and/or R.
• Experience with CDISC SDTM & ADaM standards.
• Knowledge of survival analysis, mixed models, and multiplicity control.
• Familiarity with ICH E9(R1) and regulatory submission processes.