Job Details

Overview

Principal Statistician (Remote) at Stryker shape real?world evidence (RWE) strategies across the organization. Lead statistical design and analysis for a clinical registry project, partner with surgeons and cross?functional teams, and publish impactful research.

Responsibilities

• Lead statistical analysis and methodological development for the clinical registry project, ensuring robust evidence generation from registry data.
• Partner with surgeons and clinical experts to define study questions, interpret results, and co?develop high?impact scientific outputs.
• Drive development and authorship of manuscripts, abstracts, and presentations based on registry analyses for peer?reviewed journals and international conferences.
• Provide statistical leadership in study design, analysis planning, and reporting for registry?based studies and other RWE initiatives across the portfolio.
• Advise on advanced methods for real?world data, including causal inference, survival and longitudinal modelling, and handling of complex registry datasets.
• Ensure compliance with regulatory standards, industry guidelines, and best practices for RWE study conduct.
• Represent the organization externally with academic collaborators, professional societies, and regulatory/payer bodies.
• Develop statistical analysis plans, coordinate and perform data analysis and validation as necessary, and provide data interpretation.
• Stay current with new developments in statistics, SAS programming, and regulatory guidance through literature review, conference attendance, etc.
• Perform analyses; inputs to the statistical section of the study report. Provide statistical insight into interpretation and discussion of study results.
• Develop and test SAS programs to generate data sets, tables, listings, and graphs.

Qualifications

• MS in Statistics, Biostatistics, Epidemiology, or related quantitative discipline with 8+ years of experience or PhD with 5+ years of experience.
• Expertise in registry?based research and real?world data sources.
• Strong proficiency in statistical programming (SAS, R, or Python).
• Knowledge of regulatory guidelines (FDA/CFR; ISO14155).
• Proven ability to influence study strategy and regulatory/payer discussions.
• Excellent scientific writing and presentation skills with a track record of publications.
• SAS proficiency including use of a variety of statistical procedures, e.g., nonparametric analysis, linear and non?linear models, categorical data and survival analysis.

Preferred Qualifications

• Experience supporting publication of analysis results (abstracts, posters, manuscripts).
• Advanced knowledge of registry design and analysis.
• Ability to explain statistical concepts to non?statisticians and collaborate effectively.
• Strong organizational and time management skills.

Compensation

$138,700.00 $226,900.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Benefits

Health benefits include medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program, and tobacco cessation program. Financial benefits include Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short?term disability insurance.

Job Details

Mid?Senior level, Full?time, Research, Analyst, and Information Technology. Industries: Appliances, Electrical, and Electronics Manufacturing, Industrial Machinery Manufacturing, and Medical Equipment Manufacturing.

Application

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