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Biostatistician

Propharma
2-4 years
$75,000 – $120,000
Alameda, Canada
1 June 12, 2026
Job Description
Job Type: Full Time Education: Ph.D/M.S Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill

Job Title: Biostatistician
Company: ProPharma
Location: United States / Canada
Job Type: Full-Time
Experience Required: 2–4 Years
Qualification: MS / PhD in Statistics or Related Field


Job Overview

Biostatistician role focused on clinical trial design, statistical analysis, CDISC implementation, and statistical programming support. The position supports study design, SAP development, data analysis, and regulatory submission deliverables across clinical research projects.


Key Responsibilities

Study Design & Statistical Planning

  • Interpret clinical trial protocols and statistical sections

  • Translate protocol requirements into Statistical Analysis Plans (SAPs)

  • Perform or QC sample size calculations

  • Support randomization design and specifications

Statistical Analysis & Programming

  • Develop statistical analysis plans and shells

  • Program datasets and generate statistical outputs (TLFs)

  • Conduct statistical review of clinical trial datasets

  • Support unblinding activities and treatment code integration

CDISC & Data Standards

  • Work with SDTM and ADaM datasets

  • Develop specifications for analysis datasets (CDISC-compliant)

  • Review mapping algorithms and dataset structures

  • Support standardization of clinical trial data

Quality Control & Validation

  • QC tables, listings, figures (TLFs)

  • Validate SDTM and ADaM datasets

  • Review CSR statistical sections for accuracy

  • Ensure compliance with statistical standards and protocols

Clinical Study Support

  • Support lead statistician in ongoing projects

  • Maintain TMF statistical documentation

  • Participate in project meetings and client discussions

  • Support regulatory submissions and audits


Required Skills

  • Clinical Trial Statistics

  • Statistical Analysis Planning (SAP)

  • CDISC Standards (SDTM, ADaM)

  • SAS / R Programming

  • Data Analysis & Modeling

  • Sample Size Estimation

  • Randomization Design

  • Clinical Research Knowledge

  • Quality Control (TLF validation)

  • Strong Analytical Thinking

  • Communication Skills

  • Attention to Detail