[Remote] Principal Clinical Scientist

Note: The job is a remote job and is open to candidates in USA. Beckman Coulter Diagnostics, a Danaher operating company, develops clinical diagnostic solutions for hospitals, laboratories, and physician offices worldwide. The Principal Clinical Scientist will lead clinical trial strategies in the US and EU, designing studies and evidence plans for regulatory submissions, collaborating with cross-functional teams, and overseeing clinical and regulatory documentation.

Responsibilities

• 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

Skills

• Bachelor's degree in Life Sciences, Healthcare, or a related filed with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master's degree with 6+ 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
• Ability to travel up to 10%, overnight, within US and/or EU
• Must have a valid driver's license with an acceptable driving record
• Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs
• Professional certification in Clinical Research (e.g. SoCRA, ACRP)
• Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Hematology and Urinalysis

Benefits

• This job is also eligible for bonus/incentive pay.
• Paid time off
• Medical/dental/vision insurance
• 401(k)
• This position is eligible for a remote work arrangement in which you can work remotely from your home.

Company Overview

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