Remote Biostatistician — Clinical Trials Lead

PowerToFly

Oregon (WI)

Remote

USD 120,000 - 190,000

Full time

14 days+

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Job summary

Stryker is seeking a Staff Biostatistician for a U.S.-based remote position, with preference for Eastern or Central time zones. You will lead statistical analyses across the product development lifecycle, supporting trials, regulatory submissions, and publications.

Collaboration with cross-functional teams and investigators is key as you deliver high-quality analyses and statistical outputs. The role emphasizes independent application of statistical expertise, mentoring, and contribution to

Qualifications

Master's degree in Statistics, Biostatistics, or 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.
Experience working with relational databases and clinical research data management systems.
Experience supporting scientific publications, including abstracts, posters, and peer-reviewed manuscripts.
Knowledge of FDA regulations, Good Clinical Practice (GCP), and ISO 14155 requirements.

Responsibilities

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 both technical and non-technical stakeholders.
Mentor junior statisticians and support the development of statistical standards, procedures, and best practices.