Kestra Medical Technologies Inc.
Senior Biostatistician
Kirkland, WA · Senior
No sponsorship$140k-$160kDetected 16 days ago
PythonCode ReviewSQLGCPData AnalysisData VisualizationStatisticsExcelEHR/EMRClinical TrialsClinical ResearchFDA RegulatoryMedical DevicesSASResearchExperimental DesignLeadershipCollaborationProblem SolvingCritical ThinkingAdaptabilityBiostatisticsEpidemiologyRegulatory Affairs
About the role
- This role ensures that rigorous statistical methodologies are applied to generate high-quality clinical evidence supporting Kestra products.
- Adhere to Pledge of Confidentiality Information regarding a patient of this company shall not be released to any source outside of this company without the signed permission of the patient.
- Furthermore, information will only be released internally on a need-to-know basis.
Responsibilities
- Kestra maintains a drug free workplace and testing is a
- This job description is not designed to cover or contain a comprehensive listing of activities, duties or
- Kestra maintains a drug free workplace and testing is a condition of employment.
Requirements
- Master's degree or PhD in Biostatistics, Statistics, Epidemiology, or related quantitative discipline.
- Proficiency with statistical programming tools, including SAS and/or R.
- Experience with SQL and relational database structures.
- Strong knowledge of survival analysis, regression methods, longitudinal data analysis, and observational study methodologies.
- Experience supporting scientific publications and regulatory submissions.
- Working knowledge of FDA regulations, GCP, ICH guidelines, and clinical research standards.
- Occasional lifting required, up to 20 pounds
- Occasional travel, domestic and international, may be required, less than 10%
- that are required of the Team Member.
- Applicants must be eligible to work for any employer in the U.S.
- Education/Experience Required:
- Minimum 5 years of experience supporting clinical research, clinical trials, registries, or real-world evidence studies in the medical device, biotechnology, pharmaceutical, or healthcare industry.
- Demonstrated experience in clinical study design, statistical analysis, and interpretation of clinical data.
- Ability to effectively collaborate with physicians, clinical researchers, regulatory professionals, data managers, engineers, and software teams.
- Preferred:
- Experience with medical device clinical development and post-market studies.
- Experience working with healthcare claims, EHR, registry, and other real-world data sources (e.g., Optum, HealthVerity, Truven).
Nice to have
- Experience supporting FDA submissions, post-approval studies, and international regulatory requirements.
Compensation
- Annualized at $140,000 - $160,000 plus bonus.
Benefits
- Kestra offers a very competitive benefit package including Medical, Dental, 401K with Match, etc.
- Pay equity is an important part of Kestra's Culture.
- Our compensation ranges are guided by national and local salary surveys and take into consideration experience level and internal equity.
- Salary: Annualized at $140,000 - $160,000 plus bonus.
- Kestra Medical Technologies is an
Company info
- Contagious excitement about the company - sense of urgency.
- Commitment to continuous improvement.
- We are unable to sponsor or take over sponsorship of visas (any) at this time.
Equal opportunity
- equal opportunity employer.
Visa & Work Authorization
- We are unable to sponsor or take over sponsorship of visas (any) at this time.
Apply directly at Kestra Medical Technologies Inc. →Create a free account for alerts like thisView Kestra Medical Technologies Inc. immigration profile
This listing is sourced directly from Kestra Medical Technologies Inc.'s careers page and normalized into a canonical job model.