Full-Time

Principal Statistician

Posted on 1/21/2025

Medtronic

Medtronic

10,001+ employees

Develops and manufactures medical devices and therapies

Biotechnology
Healthcare

Compensation Overview

$139.2k - $208.8kAnnually

+ Short-term Incentive Plan (MIP)

Senior, Expert

Minneapolis, MN, USA + 1 more

More locations: Boulder, CO, USA

Hybrid position requiring in-office presence.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
SAS
R
Data Analysis

You match the following Medtronic's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • Bachelor’s degree with a minimum of 7 years of statistics (i.e., biostatistics, data analysis) experience
  • An advanced degree with a minimum of 5 years of statistics (i.e., biostatistics, data analysis) experience
Responsibilities
  • Designs, plans and executes biostatistical components of plans for research and development projects that establish the conditions essential for determining safety, efficacy, and marketability of medical device products.
  • Uses sound statistical methodology to conduct studies relating to the life cycle of the product.
  • Prepares the statistical component of protocols which meet project objectives, regulatory guidelines, international standards, and clinical trial methodology standards.
  • Develops and applies statistical theories, methods, and software.
  • Summarizes and interprets data into tabular and graphical formats amenable to principles of statistical inference and is responsible for the statistical component of reports describing studies, outcomes and methods used.
  • Provides specifications and directions to the clinicians/statistical programmers.
  • Supports the regulatory review and approval of the experimental therapies.
  • Partners in trial design and in establishing standards for clinical conduct, and the collection, management and/or reporting of data.
  • Applies statistical knowledge and experience to the design of clinical studies, ensuring that study objectives can be met. This requires calculation of sample size and power, as well as determination of appropriate design assumptions from published literature.
  • Identifies potential threats to study credibility and validity, and works with study team to prevent, track, and manage potential problems.
  • Writes the statistical analysis plan for the study. Also writes and validates error-checking requirements for the study data.
  • Performs statistical analysis using statistical programming software (e.g., SAS, R etc.).
  • Takes a leadership role in responding to relevant questions from FDA, FDA Advisory Panels, and/or other regulatory agencies, and in negotiations with regulatory agencies regarding study design and interpretation, as well as in response to journal reviewer feedback.
  • Validates and provides clear documentation of analysis programs.
  • Writes Results and Methods sections of reports and manuscripts as needed and supports Discussion sections.
  • Consults with other (e.g., non-clinical) staff on statistical and analysis issues.
  • Leads development of policies and procedures for the department and the statistics group.
  • Mentors and trains Statisticians and/or Senior Statisticians in their job duties and responsibilities.
  • Attends and contributes to project and department meetings.
Desired Qualifications
  • Master's degree or PhD in Biostatistics, Statistics, or equivalent
  • 7+ years of post-graduate statistical experience
  • Experience in analysis of data from clinical studies and design of clinical trials
  • Strong applied statistical skills, including survival analysis, regression modeling, Bayesian methods, adaptive trial designs, group sequential methods, longitudinal analysis (including mixed models), interim analysis, missing data strategies and multiple testing strategies.
  • Experience with time-series analysis
  • Advanced knowledge of and/or experience with statistical programming packages, including SAS, R, or another statistical analysis package.
  • Experience communicating complex statistical/machine learning results to technical and non-technical through journal publications, conferences, presentations/posters, and seminars
  • High level of knowledge of clinical trial methods and execution.
  • Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials and medical devices (e.g., ISO, MDD/MDR).
  • Prior experience in FDA and global regulatory submissions.
  • Participation in FDA and/or Notified Body regulatory meetings, such as panel preparation and presentation, pre-sub (Q-sub) meetings, etc.
  • Presents and defends complex statistical solutions to all levels of MDT governance, key stakeholders and external regulatory bodies in a clear, concise, complete, and transparent manner that provides influence on key decisions.
  • Demonstrates excellent collaboration and interpersonal skills.
  • Demonstrated ability to communicate technical content to non-statisticians (written and verbal).
  • Experience in fast-paced working environments

Medtronic provides medical technology, services, and solutions to improve patient care. The company develops a variety of medical devices, including pacemakers, insulin pumps, surgical tools, and neurostimulation devices, which help diagnose, prevent, and treat chronic diseases. These products are used by hospitals and healthcare professionals around the world. Medtronic stands out from competitors by not only focusing on product development but also offering comprehensive services such as training for healthcare providers and patient management programs. The goal of Medtronic is to enhance patient outcomes and lower healthcare costs through its advanced medical solutions.

Company Stage

IPO

Total Funding

$3.2M

Headquarters

Fridley, Minnesota

Founded

1949

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Simplify's Take

What believers are saying

  • CE Mark approval for BrainSense™ aDBS boosts Medtronic's EU market share.
  • CMS analysis could increase adoption of Symplicity™ Spyral in the U.S.
  • Exclusive Contego agreement strengthens Medtronic's U.S. carotid market position.

What critics are saying

  • Emerging competitors like Fire1 challenge Medtronic's cardiovascular market share.
  • Exclusive agreements may limit flexibility in adapting to market changes.
  • Regulatory changes in EU could delay new product launches like BrainSense™ aDBS.

What makes Medtronic unique

  • Medtronic leads in personalized Parkinson's treatment with BrainSense™ Adaptive DBS technology.
  • The company has a strong cardiovascular portfolio, including the Symplicity™ Spyral system.
  • Medtronic's strategic partnerships enhance its orthopedic and carotid market presence.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Health Savings Account/Flexible Spending Account

Unlimited Paid Time Off

Paid Vacation

Paid Sick Leave

Paid Holidays

401(k) Retirement Plan

401(k) Company Match

Employee Stock Purchase Plan

Employee Assistance Program

Wellness Program

INACTIVE