M

MMS

Regulatory compliance and data solutions provider

Study Design Statistician

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeCanton, MI, USANo salary listedRemote

About the Job

Requirements

  • A bachelor's degree in mathematics, statistics, physics, pharmacology, or a field with a strong statistical component.
  • Five to seven years of experience applying medical statistics in pharmaceutical, contract research organization, 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.
  • Experience with SAS and/or R statistical software packages.

Responsibilities

  • Assist customers with study design, with particular focus on simulation using KerusCloud, to align studies with objectives.
  • Prepare study protocols and develop Statistical Analysis Plans and Statistical Analysis Reports.
  • Summarize, analyze, and visualize study data using a variety of statistical methods, delivering results within agreed timelines and quality standards.
  • Provide statistical consultancy support to sponsors across clinical development, including oversight of third-party statistical and programming deliverables.
  • Maintain current knowledge of relevant research techniques, including modeling, simulation, and experimental design, and participate in continuous professional development.
  • Support pre-sales discussions by identifying client needs and contributing to technical solutions and resource and cost estimates.
  • Collaborate with the Product Development team to define key features and statistical aspects of KerusCloud.
  • Provide input and support to KerusCloud marketing, including client demonstrations and white papers.

Desired Qualifications

  • A master's or PhD degree in mathematics, statistics, physics, pharmacology, or a field with a strong statistical component.
  • Experience in study design, protocol writing, and report writing.
  • Experience with modeling and simulation techniques for exploring complex study designs.
  • Experience with Bayesian approaches to the design and analysis of clinical data.
  • Experience with early-phase drug development processes, including innovative or adaptive study design.

About the Company

MMS

Regulatory compliance and data solutions provider

MMS Holdings is a global contract research organization (CRO) focused on regulatory compliance and data-driven solutions for pharmaceutical and biotech sponsors. It delivers services such as regulatory submissions, clinical trial management, data analytics, and medical writing through a service-based model that relies on established processes and experienced advisors. Its work is contract-based, often long-term, aimed at helping clients meet regulatory requirements, run trials efficiently, and advance therapies under FDA guidance. The company differentiates itself with a science-first approach, a strong track record (97% client satisfaction), and involvement in complex areas like enabling MDMA-assisted therapy research, underscoring a commitment to high-quality, compliant outcomes for sponsors globally.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Canton, Michigan
Founded
2006

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