
Senior Statistician
Posted 21 hours ago

Posted 21 hours ago
This is a fully remote position, open to applicants in Alabama, +33 more states.
• Collaborate with Medical Affairs and interdisciplinary project teams to design, plan, analyze, and interpret studies and experiments that support product development and strategic business decisions.
• Assist in the creation and review of study protocols, case report forms, as well as clinical and regulatory documentation.
• Independently create and sustain statistical analysis plans, consulting on complex or atypical situations as necessary.
• Program, document, validate, and manage statistical code in R and/or SAS for data management, analysis, visualization, and reporting purposes.
• Utilize appropriate statistical methodologies to tackle both standard and complex analytical challenges.
• Produce clear, concise, and scientifically robust statistical reports and technical documentation.
• Provide statistical analyses and insights that support project milestones across various products, platforms, and business functions.
• Remain updated on emerging statistical methodologies, industry best practices, and changing regulatory requirements.
• Present statistical results to interdisciplinary stakeholders and contribute to scientific publications, conference presentations, and external communications.
• Master’s degree in Statistics, Biostatistics, or a related quantitative field (or a comparable combination of education and experience).
• Over 3 years of experience with a Master’s degree in a regulated healthcare, life sciences, or medical device setting.
• Proven experience in applying statistical methods to product development, clinical research, and/or clinical trials.
• Proficiency in programming, documenting, and validating statistical analyses using R and/or SAS.
• Experience in independently addressing statistical and analytical challenges.
• Proven ability to lead and influence cross-functional teams without direct authority.
• Experience managing multiple projects and priorities in a fast-paced environment.
• Skilled in technical report writing and presenting statistical findings.
• Experience in stakeholder management.
• PhD in Statistics, Biostatistics, or a related quantitative discipline is preferred.
• More than 1 year of professional experience with a PhD is preferred.
• Experience in applying statistical methodologies in manufacturing, quality, regulatory, process improvement, or operational excellence initiatives.
• Knowledge of and experience working within a reproducible research environment.
• Familiarity with applicable healthcare, clinical, and medical device regulations.
• Experience in supporting submissions, regulatory interactions, or compliance-related statistical activities.
• Publication or presentation experience at scientific conferences, industry forums, or in peer-reviewed journals.
• Prior experience working across multiple product lines, business units, or global project teams.
• Demonstrated capability to foster continuous improvement through data-driven decision making and statistical innovation.
• Medical, dental, vision, health savings, and flexible spending accounts.
• Life and disability insurance.
• Wellness resources.
• Mental health support.
• Disease management programs.
• 401(k).
• Deferred compensation programs.
• Financial counseling.
• DailyPay.
• Educational savings resources.
• Paid time off.
• Company holidays.
• Educational assistance.
• Parental leave.
• Adoption assistance.
• Backup care.
• Caregiving support.
• Employee assistance programs.
• Commuter benefits.
• Pet insurance.
• Legal services.
• Associate discount programs.
• Bereavement, military, personal, family, and medical leave.
• Jury duty leave.
• Reward and recognition opportunities.
• Competitive compensation and benefits package.
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