Senior Staff Biostatistician (Remote)

Stryker Group; Las Vegas (NV); Remote; USD 100,000 - 216,000; Full time

Job summary

A leading company in neurointerventional medical devices is seeking a Senior Staff Biostatistician to drive statistical strategy for clinical trials. This remote role requires expertise in biostatistics and strong communication skills to shape clinical evidence and regulatory readiness.

Benefits

Bonus eligible

Benefits

Qualifications

• 6+ years of experience in clinical biostatistics.
• Experience with clinical trial data analysis and regulatory documentation.

Responsibilities

• Lead statistical planning and analysis for clinical trials.
• Collaborate with cross-functional teams to optimize study design.
• Provide statistical input for regulatory submissions.

Skills

SAS Programming

Statistical Concepts

Clinical Trial Data Analysis

Education

Bachelor’s degree in Biostatistics

MS or PhD in Statistics

Tools

SQL

SAS Macros

R Programming

Electronic Data Capture Systems

Job description

Stryker Neurovascular is seeking a Senior Staff Biostatistician to lead statistical strategy and execution for clinical trials supporting innovative neurointerventional medical devices. In this role, you will play a critical part in shaping clinical evidence, ensuring regulatory readiness, and advancing patient care through data-driven insights. This is a remote position to be located anywhere within the United States, preferably on the Central or Eastern time zone.

What you will do

• Lead statistical planning and analysis for clinical trials, including development of statistical analysis plans (SAPs) and interpretation of complex data

• Design and validate SAS programs to generate clinical datasets, tables, listings, and figures (TLGs) in compliance with regulatory standards

• Collaborate with cross-functional teams—including clinical scientists, regulatory affairs, and neurointerventional physicians—to optimize study design and endpoints

• Provide statistical input for regulatory submissions (e.g., FDA, EU MDR) and support clinical study reports (CSRs)

• Contribute to scientific publications and conference presentations to communicate clinical evidence

• Ensure statistical best practices across projects

• Stay current with evolving regulatory guidance and statistical methodologies relevant to medical devices

What you need

Required

• Bachelor’s degree in Biostatistics, Engineering, Science, or related field

• 6+ years of experience in clinical biostatistics

• Proficiency in SAS programming; strong ability to communicate statistical concepts to non-statisticians.

• Experience with clinical trial data analysis, inferential statistics, and regulatory documentation.

Preferred

• MS or PhD in Statistics, Mathematics, or related field

• 4+ years in medical device, pharmaceutical, or biotech settings

• Experience with SQL, SAS Macros, and electronic data capture (EDC) systems

• Experience in R programming

• Prior contributions to peer-reviewed publications or scientific presentations

• Familiarity with ISO 14155, FDA guidance, and EU MDR requirements

$100,500.00 - $215,300.00 salary plus bonus eligible + benefits. Actual minimum and maximum may vary based on location.Individual pay is based on skills, experience, and other relevant factors.