Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Biostatistician Consultant

Propharma
3+ years
$90,000 – $150,000
United States, Canada
1 June 12, 2026
Job Description
Job Type: Full Time Education: Ph.D/M.S Skills: GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment

Job Title: Senior Biostatistician Consultant
Company: ProPharma
Location: United States / Canada
Job Type: Full-Time
Experience Required: 3+ Years (Post MS/PhD)
Qualification: MS / PhD in Biostatistics or related field


Job Overview

Senior Biostatistician Consultant responsible for leading statistical design and analysis across clinical trials, ensuring high-quality statistical deliverables, regulatory compliance, and cross-functional collaboration with clinical, regulatory, and data management teams.


Key Responsibilities

Statistical Study Leadership

  • Lead statistical activities for clinical trials and research studies

  • Design study methodology and develop Statistical Analysis Plans (SAPs)

  • Provide statistical input during protocol and CRF development

  • Oversee end-to-end statistical analysis execution

Statistical Programming & Analysis

  • Develop and maintain SAS/R programs for statistical analysis

  • Ensure compliance with SOPs and regulatory standards

  • Perform analysis and generate TLFs (Tables, Listings, Figures)

  • Validate accuracy of statistical outputs and reports

Cross-Functional Collaboration

  • Provide statistical expertise to clinical operations, DM, and regulatory teams

  • Work closely with global study teams and external clients

  • Support regulatory submissions with statistical input

Quality & Compliance

  • Ensure accuracy and integrity of statistical deliverables

  • Maintain compliance with global regulatory guidelines (FDA/EMA/ICH)

  • Support development and improvement of internal SOPs and processes

Leadership & Mentoring

  • Guide and mentor junior statisticians

  • Review work of junior team members

  • Contribute to knowledge sharing and capability building


Required Skills

  • Advanced Clinical Trial Statistics

  • SAP Development & Study Design

  • SAS / R Programming (Advanced)

  • CDISC Standards (SDTM, ADaM)

  • Regulatory Guidelines (ICH, FDA, EMA)

  • Clinical Protocol Review & CRF Design

  • Statistical Modeling & Analysis

  • Strong Client Communication

  • Project Leadership & Team Mentoring

  • Problem Solving & Analytical Thinking