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Remote Statistical Programmer Jobs in Maple Grove, MN

This position is remote to enhance our competitive edge and expand our cross-functional ... Provides specifications and directions to the clinicians/statistical programmers. * Supports the ...

This position is remote to enhance our competitive edge and expand our cross-functional ... Provides specifications and directions to the clinicians/statistical programmers. * Supports the ...

This position is remote to enhance our competitive edge and expand our cross-functional ... Provides specifications and directions to the clinicians/statistical programmers. * Supports the ...

Senior Statistician - PVH

Moundsview, MN · On-site +1

$92K - $113K/yr

This position is remote to enhance our competitive edge and expand our cross-functional ... Performs statistical analysis using statistical programming software (e.g., SAS, R etc.

Senior Statistician - PVH

Moundsview, MN · On-site +1

$92K - $113K/yr

This position is remote to enhance our competitive edge and expand our cross-functional ... Performs statistical analysis using statistical programming software (e.g., SAS, R etc.

Senior Statistician - PVH

Moundsview, MN · On-site +1

$92K - $113K/yr

This position is remote to enhance our competitive edge and expand our cross-functional ... Performs statistical analysis using statistical programming software (e.g., SAS, R etc.

AI/ML Engineer

Minneapolis, MN · Remote

$106K - $131K/yr

Minneapolis, MN(Remote) 1. Design, develop, test, document, and deploy Salesforce solutions based ... MUST HAVE SKILLS 1. Bachelor's degree in Computer Science, Information Systems, Statistics, or a ...

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Remote Statistical Programmer information

See Maple Grove, MN salary details

$86.5K

$150.8K

$255K

How much do remote statistical programmer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for remote statistical programmer in Maple Grove, MN is $150,819.00, according to ZipRecruiter salary data. Most workers in this role earn between $128,000.00 and $163,800.00 per year, depending on experience, location, and employer.

What is a remote statistical programmer?

A remote statistical programmer is a professional who uses statistical software and programming languages to analyze data, typically for research, clinical trials, or business insights, while working from a location outside of a traditional office environment. They are responsible for managing, cleaning, and organizing large datasets, and for developing programs that generate statistical analyses and reports. Remote statistical programmers often collaborate with statisticians, data scientists, and project teams using online communication tools. This role requires strong skills in programming languages such as SAS, R, or Python, and attention to detail when handling complex data. Working remotely provides flexibility but also requires good time management and communication skills.

What does a remote statistical programmer do?

As a remote statistical programmer, you use programming techniques to produce useful data sets from raw data. In this role, you may evaluate the programming needs of each project, use validation techniques to ensure the accuracy of all data sets your programs make, and manage both a database and the operating environment of your software. Remote statistical programmers often work from home and collaborate with other programmers through video calls, voice chat, or remote office software. This job is also known as SAS, which stands for statistical analysis system programming, and companies may advertise under either title.

What are the key skills and qualifications needed to thrive as a remote statistical programmer, and why are they important?

To thrive as a Remote Statistical Programmer, you need strong proficiency in statistics, data analysis, and programming languages like SAS or R, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with statistical software, clinical trial data standards (such as CDISC), and regulatory submission requirements is often necessary. Attention to detail, problem-solving ability, and effective remote communication are essential soft skills for collaborating with cross-functional teams. These competencies ensure high-quality data analysis, regulatory compliance, and seamless teamwork in a remote environment.

How do remote statistical programmers typically collaborate with cross-functional teams despite working remotely?

Remote Statistical Programmers often work closely with biostatisticians, data managers, and clinical research associates using collaborative tools such as video conferencing, project management platforms, and secure data-sharing systems. Regular virtual meetings are scheduled to discuss project progress, address data or programming issues, and align on analysis plans. Clear documentation and version control are essential to ensure seamless teamwork and maintain data integrity. Effective communication skills and proactive updates help bridge the physical distance and contribute to successful project outcomes.

What is the difference between Remote Statistical Programmer vs Clinical Data Analyst?

AspectRemote Statistical ProgrammerClinical Data Analyst
Required CredentialsBachelor's/Master's in Biostatistics, Statistics, or related field; programming skills in SAS, R, or PythonBachelor's/Master's in Statistics, Data Science, or related; strong analytical and statistical skills
Work EnvironmentRemote or office-based, collaborating with biostatistics teams in clinical trialsRemote or on-site, analyzing clinical data to support study outcomes
Employer & Industry UsagePharmaceuticals, biotech, CROs, clinical research organizationsPharmaceuticals, healthcare, research institutions, CROs

Remote Statistical Programmers focus on programming and data management for clinical trials, while Clinical Data Analysts interpret and analyze clinical data. Both roles require strong statistical skills and often work in similar environments within the healthcare and pharmaceutical industries, but their core responsibilities differ.

What are popular job titles related to Remote Statistical Programmer jobs in Maple Grove, MN?

For Remote Statistical Programmer jobs in Maple Grove, MN, the most frequently searched job titles are:

What job categories do people searching Remote Statistical Programmer jobs in Maple Grove, MN look for?

The top searched job categories for Remote Statistical Programmer jobs in Maple Grove, MN are:

What cities near Maple Grove, MN are hiring for Remote Statistical Programmer jobs?

Cities near Maple Grove, MN with the most Remote Statistical Programmer job openings:

Infographic showing various Remote Statistical Programmer job openings in Maple Grove, MN as of August 2026, with employment types broken down into 55% Full Time, and 45% Part Time. Highlights an 100% Remote job distribution, with an average salary of $150,819 per year, or $72.5 per hour.

Principal Statistician - PVH

Medtronic

Moundsview, MN • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Medtronic rating

7.9

Company rating: 7.9 out of 10

Based on 180 frontline employees who took The Breakroom Quiz

154th of 545 rated manufacturers


Job description

We anticipate the application window for this opening will close on - 14 Sep 2026


Careers that change lives start here. 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 LifePeripheral Vascular Health therapies are a critical part of the Medtronic vascular portfolio, treating patients with a broad range of conditions, including Peripheral and Carotid Disease, End Stage Renal Disease, Peripheral Embolization, and Superficial and Deep Venous Disease. We lead the way in the Superficial Venous and Drug Coated Balloon markets, caring for hundreds of millions of patients globally with lifesaving and life-enhancing therapies.
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects.
The preferred location for this role is Mounds View, MN

In this exciting role as aPrincipal Statistician, you will have primary focus responsibilityfor statistical aspects of study design and analysis of data from complex clinical studies conducted for regulatory approval or marketing purposes. This includes responsibility for design of studies, calculating of sample size and power, writing of statistical portions of protocols and statistical analysis plans, review of protocol and case report forms, analysis including statistical programming and interpretation of data, and preparation of relevant sections of regulatory submissions, reports, and manuscripts. Work will generally be self-directed but will be reviewed by the manager at key time points.

Responsibilitiesmay include the following and other duties may be assigned.

  • 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.

  • Oversight of statistical support and deliverables for ensuring adherence to study specific requirements as well as consistent applications of relevant methods across the portfolio.

  • In development-phase projects, prepares the statistical component of protocols which meet project objectives, health authority guidelines, and clinical trial methodology standards.

  • Research, develop and/or applies novel 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.

  • Partner in trial design and in establishing standards for clinical trial conduct, and the collection, management and/or reporting of data.

Other responsibilities:

  • Applies statistical knowledge and experience to the design of clinical studies, ensuring that study objectives can be properly assessed. This requires calculation of sample size and power, as well as possible determination of appropriate design assumptions from published literature.

  • Assists in development and review of case report forms, ensuring data will be collected efficiently and accurately.

  • Identifies potential threats to study credibility, validity, and data integrity and works with study team to prevent, track, and manage potential problems.

  • Writes the statistical analysis plan for the study.

  • 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.

  • Uses a variety of statistical methods and software tools to analyze and display data from clinical and other studies, including more advanced methods. Methods must be appropriate for the kind of data collected and required assumptions must be tested.

  • Validates and provides clear documentation of analysis programs.

  • Writes Results and Methods sections of reports and manuscripts as needed and ensures interpretation of statistical and clinical findings in regulatory submissions, reports, and manuscripts accurately reflect the data collected.

  • Consults with other (e.g., non-clinical) staff on statistical and analysis issues.

  • Lead development for process improvements and standardization for the department and the statistics group.

  • Attends and contributes to project and department meetings.

  • Demonstrates excellent collaboration and interpersonal skills.

Must Have (Minimum Requirements):

To be considered for this role, the minimum requirements must be evident on your profile.

  • Bachelor's degree

  • Minimum of 7 years of statistical experience in clinical trial design and data analysis within healthcare

  • Advanced degree with a minimum of 5 years of statistical experience in clinical trial design and data analysis within healthcare

Nice to Have (Preferred Qualifications):

  • Master's degree or PHD degree in Biostatistics, or Statistics and minimum 8 years of statistics experience within medical device industryor pharmaceutical industries

  • Experience as a biostatistician in clinical studies from the design through approval stages in the medical deviceor pharmaceutical industries

  • Strong applied statistical skills, includingsurvival analysis, regression modeling,adaptive trial designs,group sequential methods, longitudinal analysis (including mixed models), interim analysis, Bayesian methods, missing data strategies and multiple testing strategies

  • Advanced knowledge of and/or experience withstatistical programming packages, including SAS and R

  • Participation inFDA, PMDA or otherregulatory meetings, especially panel preparation and presentation

  • Experience inGood Clinical Practice (GCP)and/or regulatory compliance guidelines for clinical trialsand medical devices (e.g.,ISO, MDD/MDR)

  • High level of knowledge of clinical trial methods and execution

  • High degree of expertise regarding research data management

  • High level of competency in Windows environment and with Microsoft Office Tools (Word, Excel)

  • Demonstrated ability to communicate technical content to non-statisticians (written and verbal)

  • Experience writing or updating clinical reports/documents

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

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:


Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.


Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.


If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.


If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$146,400.00 - $219,600.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others)

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance,Health Savings Account,Healthcare Flexible Spending Account,Life insurance, Long-term disability leave,Dependent daycare spending account,Tuition assistance/reimbursement, andSimple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees:Incentive plans, 401(k) plan plus employer contribution and match,Short-term disability,Paid time off,Paid holidays,Employee Stock Purchase Plan,Employee Assistance Program,Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), andCapital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.


If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can findhere a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.


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