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Remote Clinical Trial Transparency Jobs in Michigan

Stryker

Staff Biostatistician (Remote)

Portage, MI · On-site +1

$124K - $207K/yr

This role combines statistical leadership, clinical trial support, and scientific collaboration to ... S. work location and transparency guide to find the pay range for your location. Travel Percentage ...

Becton, Dickinson and Company

... remote). * Actively participate in site feasibility assessments and site selection processes ... Strong understanding of clinical trial operations, monitoring practices, investigational product ...

New

Alumis

Medical Science Liaison

Detroit, MI · On-site +1

$19K/yr

The MSL will engage with HCPs to support trial enrollment, educate on disease states and clinical ... Experience in a start-up environment is a plus This position is primarily remote. The salary range ...

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Remote Clinical Trial Transparency information

What are some common challenges faced by professionals in a remote clinical trial transparency role, and how can they be addressed?

Professionals in Remote Clinical Trial Transparency roles often encounter challenges such as managing large volumes of sensitive data, ensuring regulatory compliance across multiple jurisdictions, and coordinating with global stakeholders virtually. Effective organization, strong communication skills, and staying up to date with evolving regulations are key to addressing these challenges. Utilizing secure data management platforms and fostering clear communication channels with cross-functional teams can help ensure both transparency and compliance in a remote environment.

What are the key skills and qualifications needed to thrive as a remote clinical trial transparency specialist?

To thrive as a Remote Clinical Trial Transparency Specialist, you need a solid understanding of clinical research processes, regulatory requirements (like FDA, EMA, or ICMJE), and often a degree in life sciences or healthcare. Familiarity with trial disclosure platforms (such as ClinicalTrials.gov and EudraCT), document management systems, and data anonymization tools is typically required. Strong attention to detail, analytical thinking, and effective written communication are crucial soft skills for ensuring accuracy and compliance. These abilities are vital to uphold regulatory standards, protect patient privacy, and promote trust through transparent clinical trial reporting.

What is a remote clinical trial transparency professional?

A Remote Clinical Trial Transparency professional is responsible for ensuring that information about clinical trials is accurately disclosed and made accessible to the public, regulators, and other stakeholders while working remotely. Their work involves preparing, reviewing, and submitting clinical trial data, maintaining compliance with global regulations, and protecting patient confidentiality. They ensure transparency by posting trial results to public registries, responding to disclosure requests, and supporting ethical standards in clinical research.

What is the difference between Remote Clinical Trial Transparency vs Remote Clinical Data Manager?

AspectRemote Clinical Trial TransparencyRemote Clinical Data Manager
Primary FocusEnsuring transparency of clinical trial results and compliance with reporting regulationsManaging and cleaning clinical trial data for analysis and reporting
Required CredentialsRegulatory knowledge, clinical trial experience, often a degree in life sciencesBiostatistics, data management certifications, degree in health sciences or related field
Work EnvironmentRemote, regulatory agencies, pharmaceutical companies, CROsRemote, pharmaceutical companies, CROs, data management teams

While both roles operate remotely within the clinical research industry, Remote Clinical Trial Transparency focuses on reporting compliance and transparency of trial results, whereas Remote Clinical Data Managers handle the technical aspects of data collection and management. Both require knowledge of clinical processes but serve different functions in the clinical trial lifecycle.

What are the most commonly searched types of Clinical Trial Transparency jobs in Michigan?

The most popular types of Clinical Trial Transparency jobs in Michigan are:

What are popular job titles related to Remote Clinical Trial Transparency jobs in Michigan?

For Remote Clinical Trial Transparency jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Trial Transparency jobs in Michigan look for?

The top searched job categories for Remote Clinical Trial Transparency jobs in Michigan are:

What cities in Michigan are hiring for Remote Clinical Trial Transparency jobs?

Cities in Michigan with the most Remote Clinical Trial Transparency job openings:

Remote Clinical Trial Transparency jobs near you
Infographic showing various Remote Clinical Trial Transparency job openings in Michigan as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% Remote job distribution.

Staff Biostatistician (Remote)

Stryker

Portage, MI • On-site, Remote

$124K - $207K/yr

Full-time

Posted 9 days ago

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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