Principal Clinical Scientist

Principal Clinical Scientist

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

This position reports to the Senior Manager, Clinical Science and is part of Beckman Coulter, Inc. Hematology and Urinalysis business unit located in Miami, FL and will be fully remote.

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, CE IVDR) 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 cross functionally 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 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.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel up to 10%, overnight, within US and/or EU
• Must have a valid driver's license with an acceptable driving record

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 Hematology and Urinalysis
• Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs
• Professional certification in Clinical Research (e.g. SoCRA, ACRP)

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.