Principal Clinical Scientist
Chaska, MN · On-site +1
You will drive strategic study designs, ensuring regulatory compliance, and achieving key ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
Chaska, MN · On-site +1
You will drive strategic study designs, ensuring regulatory compliance, and achieving key ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
Chaska, MN · On-site +1
You will drive strategic study designs, ensuring regulatory compliance, and achieving key ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
This position is Remote in Eastern, Central, OR Mountain Time Zone. You will have the flexibility ... time studies (along with oversight by supervisor and manager) * Assist with follow up and/or ...
This position is Remote in Eastern, Central, OR Mountain Time Zone. You will have the flexibility ... time studies (along with oversight by supervisor and manager) * Assist with follow up and/or ...
This position is Remote in Eastern, Central and Mountain time zones. You will have the flexibility ... time studies (along with oversight by supervisor and manager) * Assist with follow up and/or ...
This position is Remote in Eastern, Central and Mountain time zones. You will have the flexibility ... time studies (along with oversight by supervisor and manager) * Assist with follow up and/or ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Rochester, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Saint Paul, MN · Remote
$50 - $80/hr
Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ...
Minneapolis, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Minneapolis, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Rochester, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Rochester, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Saint Paul, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Saint Paul, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Rochester, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Rochester, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Saint Paul, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Saint Paul, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Minneapolis, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
Minneapolis, MN · Remote
$60 - $100/hr
Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Demonstrated command of clinical study design, regulatory documentation, and observational research ...
This position is remote. Our ideal candidate will reside near our headquarters in Brooklyn Park, MN ... Becomes proficient with all study databases, systems and company quality management system
This position is remote. Our ideal candidate will reside near our headquarters in Brooklyn Park, MN ... Becomes proficient with all study databases, systems and company quality management system
Minneapolis, MN · Remote
$60 - $65/hr
Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...
Minneapolis, MN · Remote
$60 - $65/hr
Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... study reports (CSR), including subtle errors in population definitions, censoring rules, or ...
| Aspect | Remote Clinical Study Startup | Remote Clinical Trial Coordinator |
|---|---|---|
| Primary Role | Planning and initiating clinical studies, including site selection and regulatory submissions | Managing daily trial activities, site communication, and data collection |
| Required Credentials | Typically a background in life sciences, clinical research certifications preferred | Similar credentials, often with clinical research or coordinator certifications |
| Work Environment | Primarily remote, collaborating with sponsors, CROs, and sites | Remote or hybrid, focusing on site management and data oversight |
| Industry Usage | Used during study initiation phase | Used during trial execution phase |
Remote Clinical Study Startup involves planning and launching new clinical trials, while Remote Clinical Trial Coordinator focuses on managing ongoing trial activities. Both roles require similar credentials and often operate remotely within the clinical research industry, but they differ in their specific responsibilities and timing within the study lifecycle.
The most popular types of Clinical Study Startup jobs in Minnesota are:
For Remote Clinical Study Startup jobs in Minnesota, the most frequently searched job titles are:
The top searched job categories for Remote Clinical Study Startup jobs in Minnesota are:
Cities in Minnesota with the most Remote Clinical Study Startup job openings:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 24 days ago
7.7
Based on 31 frontline employees who took The Breakroom Quiz
199th of 539 rated manufacturers
At Danaher Diagnostics, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.
Danaher Diagnostics is a community of six companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.
Learn about the Danaher Business System which makes everything possible.
Principal Clinical Scientist. This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics. This role will specifically support Beckman Coulter Diagnostics and Life Sciences, operating companies of Danaher Diagnostics. You will drive strategic study designs, ensuring regulatory compliance, and achieving key milestones for critical clinical studies in these vital markets.
This position is part of the Danaher Diagnostics, Beckman Coulter Inc. organization and will be located on-site at either Chaska, MN or Miami, FL. At Danaher Diagnostics, our vision is to be the leading provider of seamlessly connected diagnostic solutions.
In this role, you will have the opportunity to:
Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA 510(k)/PMA, CEIVDR) across multiple diagnostic modalities.
Act as a scientific and clinical liaison with regulatory bodies, key opinion leaders, and external sites to develop protocols, claims, and evidence plans.
Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align clinical programs with product development and market access needs.
Author and review clinical and regulatory documentation-including study reports, technical files, and publications-to support product clearance and commercialization.
Build strong internal and external collaborations, mentor junior scientists, and maintain expertise in evolving regulatory standards, clinical guidelines, and diagnostic technologies.
The essential requirements of the job include:
Bachelor's degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master's degree with 12+ years of experience or Doctoral degree with 4+ years of same experience.
In-depth understanding of clinical study design and methodology in the diagnostics, medical device, or pharmaceutical industry with products intended for the US and EU markets.
Demonstrated ability to identify and solve complex issues in clinical trial conduct and scientific interpretation.
Ability to critically review and interpret scientific and clinical trial data, and oversee the scientific aspects of study protocols and reports.
Excellent communication (written and verbal) and interpersonal skills for collaborating with cross-functional stakeholders.
It would be a plus if you also possess previous experience in:
Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Clinical Chemistry, Immunoassays, Hematology, Urinalysis, Flow Cytometry, and/or Biomarkers.
Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs.
Professional certification in Clinical Research (e.g., SoCRA, ACRP).
Danaher Diagnostics, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.
This job is also eligible for bonus/incentive pay.
WithinDanaherDiagnosticswe believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that workingwithinDanaherDiagnosticscan provide.
Theannualsalary range for this role is $120K-$165K.This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit www.danaher.com.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here.
For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.
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We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.
Medical equipment and supplies manufacturing
10,000+ Employees
Washington, DC, US
1984