Staff Biostatistician

🕒 August 4

🚗 Michigan – Remote

🚗 Michigan – Remote

💵 $95.7k - $207.4k / year

⏰ Full Time

🔴 Lead

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 23%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Stryker

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1941

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.

📋 Description

• 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 • Support the design, analysis, and interpretation of clinical research data across the product development lifecycle • Serve as a key statistical expert for assigned studies and deliver accurate, timely statistical outputs for internal and external stakeholders

🎯 Requirements

• 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

🏖️ Benefits

• Remote work flexibility • 10% travel percentage