Statisticien

## Statisticien Postuler:
Sur site:
Minneapolis, Minnesota, United States of America:
Temps plein:
Offre publiée hier:
Date de fin : 27 octobre 2026 (Il reste 6 jour(s) pour postuler):
R79230

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

Chez Medtronic, vous pouvez entamer une longue carrière d’exploration et d’innovation tout en aidant à soutenir l’accès aux soins de santé et l’équité pour tous. Vous dirigerez avec détermination en surmontant les obstacles à l’innovation dans un monde davantage connecté et compatissant.
** Journée type
** 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.
** Primary Responsibilities*
* * 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.
** Required Qualifications*
* * 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.  
** Preferred Qualifications
*** 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.
* Experience communicating statistical concepts and study results to technical and non-technical audiences.

Pour les diplômes de baccalauréat obtenus en dehors des États-Unis, un diplôme qui satisfait aux exigences de la réglementation 8 C.F.R. § 214.2…