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MMS

Study Design Statistician

MMS

Statistician offering statistical expertise for clinical trial design and analysis. Engaging with clients and contributing to the development of innovative solutions in a supportive environment.

Posted 4/21/2026full-timeRemote • Missouri • 🇺🇸 United StatesMid-LevelSeniorWebsite

About the role

Key responsibilities & impact
  • Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives.
  • Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports.
  • Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality.
  • Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables.
  • Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity.
  • Support pre-sales discussions to understand and identify client needs, then contribute to technical solutions and resource/ cost estimates.
  • Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud.
  • Provide input and support to Marketing of KerusCloud, including demonstrations to clients, white papers, etc.

Requirements

What you’ll need
  • Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred.
  • 5-7 years of experience in the application of medical statistics (pharma, CRO, academic).
  • Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions.
  • Experience in delivering customer projects to high quality standards.
  • Experience in SAS and/ or R statistical software packages.
  • Experience in study design and protocol and report-writing preferred.
  • Experience of modelling and simulation techniques to explore complex study designs preferred.
  • Experience of Bayesian approaches to design and analysis of clinical data preferred.
  • Experience of early-phase drug development processes including innovative/ adaptive study design preferred.

Benefits

Comp & perks
  • supportive, innovative team
  • Great Place to Work certified organization
  • exceptional culture and industry best employee retention rate

ATS Keywords

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Hard Skills & Tools
statistical analysisstudy designprotocol writingreport writingmodelling techniquessimulation techniquesBayesian analysisclinical data analysisstatistical consultancyproject delivery
Soft Skills
client engagementproblem solvingcreative solutionsbusiness orientationcollaborationcommunicationquality assurancecontinuous professional development
Certifications
Bachelor's degreeMaster's degreePhD