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Remote Program Evaluation Jobs in Michigan (NOW HIRING)

Staff Biostatistician (Remote)

Portage, MI · On-site +1

$124K - $207K/yr

... programs, evaluate study data, develop analytical strategies, and deliver accurate, timely ... data evaluation. * Collaborate with clinical, data management, regulatory, and research teams to ...

Proactively assesses market risks and opportunities, evaluating multiple possible solutions, and ... new products, programs, and processes. * This role may require occasional travel ( Required ...

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Remote Program Evaluation information

What is a remote program evaluation?

A Remote Program Evaluation job involves assessing the effectiveness, efficiency, and impact of programs from a remote location. Professionals in this role collect and analyze data, generate reports, and provide recommendations to improve program outcomes. They may use surveys, interviews, and statistical methods to evaluate performance. This position is common in nonprofits, corporations, and government agencies that need to measure program success. Strong analytical skills, attention to detail, and experience with evaluation methodologies are essential for success in this role.

What are the typical responsibilities of a remote program evaluation professional?

As a Remote Program Evaluation professional, your primary responsibilities include designing and implementing evaluation plans, collecting and analyzing quantitative and qualitative data, and generating comprehensive reports on program effectiveness. You may also facilitate virtual interviews or focus groups, collaborate with stakeholders to refine evaluation objectives, and use digital tools for data visualization and communication. The role often involves working independently, but you will regularly coordinate with program managers, data analysts, and other team members to ensure evaluation goals are met. This structure allows for flexible work hours while still contributing valuable insights to drive program improvements.

What are the key skills and qualifications needed to thrive in remote program evaluation?

To thrive in Remote Program Evaluation, you need strong analytical, research, and data interpretation skills, typically supported by a background in social sciences, public health, education, or related fields. Familiarity with evaluation frameworks, statistical software (such as SPSS or R), and data management tools is highly valuable, as are certifications like the Certified Evaluation Professional (CEP). Excellent written and verbal communication, self-motivation, and attention to detail enhance your ability to collaborate across remote teams and present findings effectively. These skills ensure accurate program assessments, actionable recommendations, and successful outcomes in a virtual working environment.

What job categories do people searching Remote Program Evaluation jobs in Michigan look for?

The top searched job categories for Remote Program Evaluation jobs in Michigan are:

What cities in Michigan are hiring for Remote Program Evaluation jobs?

Cities in Michigan with the most Remote Program Evaluation job openings:

Infographic showing various Remote Program Evaluation job openings in Michigan as of August 2026, with employment types broken down into 5% Internship, 70% Full Time, 20% Part Time, and 5% Contract. Highlights an 100% Remote job distribution.

Staff Biostatistician (Remote)

Portage, MI • On-site, Remote

Stryker
Medical Equipment and Supplies Manufacturing • 10K+ employees

$124K - $207K/yr

Full-time

Re-posted 10 days ago


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz


Job description

Work Flexibility: Remote

Stryker is seeking a Staff Biostatistician to join our Instruments division. This is a U.S.-based remote position, with preference for candidates located in the Eastern or Central time zones.

As the Staff Biostatistician, you will support the design, analysis, and interpretation of clinical research data across the product development lifecycle. This role combines statistical leadership, clinical trial support, and scientific collaboration to ensure high-quality analyses that inform research, regulatory submissions, publications, and business decisions. You will work closely with cross-functional teams and clinical investigators while serving as a key statistical expert for assigned studies.

This individual contributor role requires independent application of statistical expertise to support clinical research programs, evaluate study data, develop analytical strategies, and deliver accurate, timely statistical outputs for internal and external stakeholders.

What You Will Do

  • Develop statistical analysis plans, including methodology, derived variables, data handling rules, analysis populations, and table, listing, and figure specifications.

  • Lead statistical support for clinical trials by analyzing study data and generating statistical outputs, reports, and study deliverables.

  • Contribute statistical content to clinical trial protocols, regulatory documentation, study reports, and scientific publications.

  • Perform statistical analyses using SAS and other analytical tools to support clinical research, operational metrics, and data-driven decision-making.

  • Design and evaluate technical solutions, databases, and analytical processes that improve clinical trial execution and data evaluation.

  • Collaborate with clinical, data management, regulatory, and research teams to support protocol design, study conduct, and interpretation of results.

  • Present statistical findings to project teams and explain analysis methods and outcomes to both technical and non-technical stakeholders.

  • Mentor junior statisticians and support the development of statistical standards, procedures, and best practices.

What You Need

Required

  • Master's degree in Statistics, Biostatistics, or a related quantitative field with medical research content.

  • Minimum 4 years of relevant biostatistics experience, inclusive of postgraduate experience.

  • Experience supporting clinical trials through statistical analysis plan development, data analysis, and reporting.

  • Knowledge of clinical trial design, statistical methodologies, and regulatory requirements applicable to clinical research.

Preferred

  • Proficiency with SAS analytical software.

  • Experience working with relational databases and clinical research data management systems.

  • Experience supporting scientific publications, including abstracts, posters, and peer-reviewed manuscripts.

  • Knowledge of FDA regulations, Good Clinical Practice (GCP), and ISO 14155 requirements.

United States of America Pay Ranges:

  • USN: $95,700 - $159,500 USD Annual
  • US5: $100,500 - $167,500 USD Annual
  • US10: $105,300 - $175,500 USD Annual
  • US15: $110,100 - $183,400 USD Annual
  • US20: $114,800 - $191,400 USD Annual
  • US30: $124,400 - $207,400 USD Annual

View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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