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Clinical Development Scientist Jobs in Ohio (NOW HIRING)

Our associates are involved in every stage of diagnostics, from ideation to development and ... Principal Clinical Scientist . This role is responsible for clinical trial strategies within the US ...

... lV clinical development services to the biotechnology, pharmaceutical, and medical device ... Work alongside physicians, scientists, and industry-leading experts committed to advancing the ...

... lV clinical development services to the biotechnology, pharmaceutical, and medical device ... Work alongside physicians, scientists, and industry-leading experts committed to advancing the ...

Provide strategic scientific and medical leadership for CNS and Psychiatry development programs spanning Phase I through late-stage clinical development, ensuring robust clinical, regulatory, and ...

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

$68.52 - $85.65/hr

You will work closely with Translational Research, Clinical Development, Clinical Operations ... University degree in life sciences, biomedical sciences, clinical research, biotechnology, pharmacy ...

New

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Collaborative Culture

Showing results 21-40

Clinical Development Scientist information

See Ohio salary details

$26

$52

$77

How much do clinical development scientist jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical development scientist in Ohio is $52.05, according to ZipRecruiter salary data. Most workers in this role earn between $38.17 and $64.90 per hour, depending on experience, location, and employer.

What does a clinical development scientist do?

A Clinical Development Scientist is responsible for designing, planning, and overseeing clinical trials that test new drugs, therapies, or medical devices. They collaborate with cross-functional teams to ensure that clinical studies are scientifically sound, compliant with regulations, and aligned with strategic objectives. Their work involves protocol development, data analysis, and interpretation of results to support regulatory submissions and product approvals. Ultimately, they play a key role in bringing safe and effective treatments to patients.

What skills and qualifications are needed to be a clinical development scientist?

To thrive as a Clinical Development Scientist, you need a solid background in life sciences, clinical research methodologies, and drug development, often supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory requirements, clinical trial management systems (CTMS), and data analysis tools is essential. Strong analytical thinking, attention to detail, and effective communication skills help you collaborate cross-functionally and drive successful clinical studies. These skills ensure rigorous study design, regulatory compliance, and effective advancement of new therapies through clinical pipelines.

How does a clinical development scientist collaborate with cross-functional teams during a clinical trial?

Clinical Development Scientists play a central role in coordinating with various teams such as clinical operations, regulatory affairs, data management, and biostatistics throughout a clinical trial. They ensure that clinical protocols are scientifically sound and align with regulatory requirements, while also facilitating clear communication between departments to address study challenges and maintain timelines. By serving as the scientific point of contact, they help integrate input from multiple stakeholders, support troubleshooting during trial execution, and contribute to the preparation of study documents and data analysis.

What is the difference between Clinical Development Scientist vs Clinical Research Associate?

AspectClinical Development ScientistClinical Research Associate
Required credentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's in Life Sciences or related field, often with certification in clinical trials
Work environmentDesigning and planning clinical trials, collaborating with teamsMonitoring clinical trials at sites, ensuring protocol compliance
Employer and industry usagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, research institutions
Common search and comparison intentUnderstanding roles in clinical developmentMonitoring and managing clinical trial sites

The Clinical Development Scientist focuses on designing, planning, and analyzing clinical trials, working closely with research teams. In contrast, the Clinical Research Associate primarily monitors trial sites to ensure compliance and data integrity. Both roles are essential in clinical research but differ in responsibilities and daily tasks.

What job categories do people searching Clinical Development Scientist jobs in Ohio look for?

The top searched job categories for Clinical Development Scientist jobs in Ohio are:

Infographic showing various Clinical Development Scientist job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $108,263 per year, or $52 per hour.

Principal Clinical Scientist

Danaher

Cleveland, OH • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

191st of 545 rated manufacturers


Job description

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 remote based (can also be onsite in Chaska, MN). 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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About Danaher

Sourced by ZipRecruiter

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.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984