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Study Design Statistician; Remote

Remote / Online - Candidates ideally in
Michigan, USA
Listing for: MMS
Remote/Work from Home position
Listed on 2026-07-14
Job specializations:
  • Research/Development
    Research Scientist, Data Scientist
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR
Job Description & How to Apply Below
Position: Study Design Statistician (Remote)

Role Overview

Strategic Statistician – full‑time role focusing on clinical trial design, consulting, and internal/external SME for statistical services within MMS’s Strategic Statistical Services Arm.

Responsibilities
  • Assist customers with study design, focusing on Kerus Cloud simulation to align with study objectives.
  • Prepare study protocols and develop Statistical Analysis Plans and Reports.
  • Summarize, analyze, and visualize study data using statistical methods, delivering results within agreed timelines and quality standards.
  • Provide statistical consultancy support to sponsors across clinical development, overseeing third‑party statistical and programming deliverables.
  • Maintain up‑to‑date knowledge of relevant research techniques (modeling, simulation, experimental design) and participate in continuous professional development.
  • Support pre‑sales discussions to understand and identify client needs, contribute to technical solutions and resource/cost estimates.
  • Collaborate with product development to define key features and statistical aspects of Kerus Cloud.
  • Provide input and support to marketing of Kerus Cloud, including demonstrations to clients and white papers.
Requirements
  • Bachelor’s degree in mathematics, statistics, physics, pharmacology, or a related field with a strong statistical component;
    Master’s or PhD preferred.
  • 5–7 years of experience applying medical statistics in pharma, CRO, or academic settings.
  • Willingness to engage with clients to understand and research problems and provide creative, business‑oriented solutions.
  • Experience delivering customer projects to high‑quality standards.
  • Proficiency in SAS and/or R statistical software packages.
  • Experience in study design, protocol and report writing preferred.
  • Experience in modeling and simulation techniques for complex study designs preferred.
  • Experience with Bayesian approaches to design and analysis of clinical data preferred.
  • Experience in early‑phase drug development processes, including innovative/adaptive study designs, preferred.
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