Staff Biostatistician

Stryker

Staff Biostatistician supporting Stryker’s medical-device clinical research and product development. Designing analyses, interpreting trial data, and contributing to regulatory submissions and publications.

Posted 8/4/2026full-timeRemote • Missouri • 🇺🇸 United StatesLead💰 $95,700 - $207,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Expertise in statistical analysis and clinical trial support, with a strong foundation in SAS programming, biostatistics, and regulatory compliance. Proven ability to collaborate across teams and mentor junior staff while contributing to scientific publications and improving clinical research methodologies.

Highest-signal resume keywords

Master’s Degree In StatisticsBiostatistics ExperienceSAS Analytical SoftwareClinical Trial Design KnowledgeFDA Regulations Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical Analysis PlansData AnalysisStatistical MethodologiesData Handling RulesStatistical OutputsClinical ResearchTechnical Solutions DesignData EvaluationStatistical ReportingRelational Databases

Soft Skills

CollaborationMentoringCommunication

Tools & Technologies

SASClinical Research Data Management Systems

Industry Keywords

Good Clinical Practice (GCP)ISO 14155Regulatory DocumentationScientific PublicationsStudy Protocols

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Develop statistical analysis plans, including methodology, derived variables, data handling rules, analysis populations, and table, listing, and figure specifications
Lead statistical support for clinical trials by analyzing study data and generating statistical outputs, reports, and study deliverables
Contribute statistical content to clinical trial protocols, regulatory documentation, study reports, and scientific publications
Perform statistical analyses using SAS and other analytical tools to support clinical research, operational metrics, and data-driven decision-making
Design and evaluate technical solutions, databases, and analytical processes that improve clinical trial execution and data evaluation
Collaborate with clinical, data management, regulatory, and research teams to support protocol design, study conduct, and interpretation of results
Present statistical findings to project teams and explain analysis methods and outcomes to technical and non-technical stakeholders
Mentor junior statisticians and support the development of statistical standards, procedures, and best practices

Requirements

What you’ll need

Required Master’s degree in Statistics, Biostatistics, or a related quantitative field with medical research content
Minimum 4 years of relevant biostatistics experience, inclusive of postgraduate experience
Experience supporting clinical trials through statistical analysis plan development, data analysis, and reporting
Knowledge of clinical trial design, statistical methodologies, and regulatory requirements applicable to clinical research
Proficiency with SAS analytical software preferred
Experience working with relational databases and clinical research data management systems preferred
Experience supporting scientific publications, including abstracts, posters, and peer-reviewed manuscripts preferred
Knowledge of FDA regulations, Good Clinical Practice (GCP), and ISO 14155 requirements preferred
U.S.-based work location
Preference for candidates located in Eastern or Central time zones

Benefits

Comp & perks

Remote work arrangement
Annual salary range of $95,700–$207,400 USD depending on U.S. work location
10% travel percentage