Statistician -Medtronic Clinical Research Solutions; MCRS; On-site

We anticipate the application window for this opening will close on - 27 Oct 2026

Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life Medtronic Clinical Research Solutions (MCRS) provides end-to-end clinical and scientific support services across Medtronic, enabling the execution of clinical studies and delivery of clinical statistical services that support evidence generation throughout the product lifecycle. This team partners with clinical, regulatory, data management, and statistical programming functions to generate high-quality clinical evidence that informs product development and regulatory submissions.

This position is based in Minnesota and is expected to work onsite four days per week. The role supports global clinical research activities and requires up to 10% travel, primarily domestic with occasional international travel. The Statistician - MCRS supports clinical research studies through statistical design, analysis, interpretation, and reporting of clinical data. This role partners with cross‑functional teams to develop statistical approaches for clinical investigations, contribute to study planning and execution, and deliver analyses that support product development and regulatory objectives.

• Design and execute statistical analyses for clinical research studies evaluating the safety and effectiveness of medical devices.
• Develop statistical sections of clinical study protocols and analysis plans aligned with study objectives and regulatory requirements.
• Program, validate, and perform statistical analyses using SAS and/or R to support clinical evidence generation.
• Analyze, summarize, and interpret clinical data, delivering statistical outputs, reports, and study results for internal and regulatory stakeholders.
• Partner with clinical, regulatory, data management, and statistical programming teams to support study execution and submission activities.
• Provide statistical guidance on study design, data collection, reporting standards, and regulatory interactions.

• Bachelor's degree and 2+ years of biostatistics, statistics, epidemiology, or clinical research experience OR Master's degree and 0+ years of experience.
• Experience applying statistical methods to clinical, healthcare, or research data.
• Experience with SAS and/or R programming.
• Experience analyzing and interpreting data and presenting results through tables, figures, and statistical reports.
• Experience communicating statistical concepts and study results to technical and non‑technical audiences.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8C.F.R. §214.2(h)(4)(iii)(A) is required.

• Master's degree in Biostatistics, Statistics, or Epidemiology.
• Experience supporting clinical research within a Clinical Research Organization (CRO), medical device, pharmaceutical, or biotechnology environment.
• Knowledge of Good Clinical Practice (GCP) and medical device or clinical trial regulatory requirements, including ISO, Medical Device Directive (MDD), or Medical Device Regulation (MDR).
• Experience with clinical research data management and relational databases.
• Proficiency with Microsoft Office applications, including Excel and Word.

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