Work Flexibility: Remote or Hybrid or Onsite

As a Principal Biostatistician, you will play a critical role in shaping real-world evidence (RWE) strategies across the organization. You will lead statistical design and analysis for our clinical registry project—a cornerstone initiative for understanding long-term clinical outcomes. This role partners closely with surgeons, clinical experts, and cross-functional teams to generate high-quality evidence, publish impactful research, and present findings at scientific meetings.

What You Will Do

Lead the 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 the 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.

What You Need

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

Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.