Remote Biostatistics Consultant | Part-Time | 6-Month Contract

Sigma Systems is seeking an experienced Remote Biostatistics Consultant to support statistical deliverables for an oncology clinical research program. This part-time consulting opportunity is ideal for a biostatistician with strong clinical trial experience, advanced statistical expertise, and the ability to collaborate with cross-functional teams to deliver high-quality, publication-ready analyses.

Job Details

Position: Biostatistics Consultant
Location: Remote
Employment Type: Part-Time Contract
Contract Duration: 6 Months

Work Schedule:

• First 3 months: Approximately 10–15 hours per week
• Remaining contract period: Approximately 5–10 hours per week

Overview

The Biostatistics Consultant will serve as a key statistical partner supporting oncology clinical trial activities. The consultant will review and finalize analysis datasets, validate statistical analyses, support data quality initiatives, generate statistical outputs, and contribute to publication-related materials.

This role will work closely with medical strategy leaders, publication specialists, statistical programmers, and cross-functional research teams to ensure analyses are scientifically rigorous, accurate, and ready for regulatory and publication use.

Key Responsibilities

• Serve as the primary biostatistical resource supporting study closeout activities
• Review, validate, and execute statistical analyses for clinical trial data
• Review and finalize analysis datasets for accuracy and consistency
• Conduct data quality checks and identify potential data issues
• Provide statistical guidance to programming teams developing:
  • SDTM and ADaM datasets
  • Tables, Listings, and Figures (TLFs)
  • Statistical specifications and analysis outputs
• Perform quality control reviews of statistical programming deliverables
• Generate and interpret statistical tables, figures, and listings
• Apply advanced statistical methodologies to oncology clinical trial data
• Support statistical content development for publications and scientific communications
• Communicate complex statistical concepts clearly to technical and non-technical stakeholders
• Collaborate with cross-functional teams to address publication and analysis-related questions
• Provide data-driven insights and recommendations to project teams

Required Qualifications

• Master’s or PhD degree in Statistics, Biostatistics, or a related quantitative field
• Clinical trial experience:
  • Approximately 3+ years for PhD candidates
  • Approximately 5+ years for MS candidates
• Strong understanding of statistical principles, clinical trial design, and modern statistical methodologies
• Experience applying statistical methods in oncology clinical trials
• Strong written and verbal communication skills
• Ability to explain complex statistical concepts, methodologies, and analysis plans to diverse audiences
• Experience with Bayesian modeling and Bayesian analysis
• Proficiency with statistical programming tools including:
  • SAS
  • R
  • Other statistical analysis software

Preferred Experience

• Experience with CDISC data standards including:
  • SDTM
  • ADaM
• Experience reviewing statistical programming specifications and outputs
• Experience supporting clinical publications and scientific manuscripts
• Strong attention to detail and commitment to data integrity