Remote Principal Clinical Scientist - Neurodegenerative

Beckman Coulter Diagnostics; Las Vegas (NV); Hybrid; USD 120,000 - 130,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

Beckman Coulter Diagnostics, a Danaher company, is seeking a Principal Clinical Scientist to lead clinical trial strategies for US and EU regions across diagnostic modalities. You will drive regulatory compliance and milestone achievement for critical studies in global markets.

This role involves study design, regulatory liaison, and collaboration with Regulatory, R&D, Medical Affairs, Quality, and Commercial teams, while mentoring junior scientists and staying current with guidelines and

Qualifications

• Bachelor’s degree in Life Sciences, Healthcare, or related field with 9+ years in clinical research.
• Understanding of clinical study design in diagnostics/medical devices/pharma for US/EU.
• Ability to identify and solve complex issues in trial conduct and interpretation.
• Ability to review and interpret clinical data and oversee study protocols/reports.
• Excellent written and verbal communication for cross‑functional collaboration.

Responsibilities

• Design clinical studies and evidence strategies for global regulatory submissions (FDA 510(k)/PMA, CE‑IVDR).
• Act as liaison with regulatory bodies, KOLs, and external sites to develop protocols and evidence plans.
• Partner with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align programs with product needs.
• Author and review clinical and regulatory documents, including study reports and publications.
• Build internal/external collaborations, mentor junior scientists, stay updated on regulatory standards and diagnostic tech.

Skills

Clinical research

Regulatory submissions

Cross-functional collaboration

Scientific writing

Education

Bachelor's degree in Life Sciences

Master's degree

Doctoral degree

Job description

Beckman Coulter Diagnostics, a Danaher company, is seeking a Principal Clinical Scientist to lead clinical trial strategies for US and EU regions across diagnostic modalities. You will drive regulatory compliance and milestone achievement for critical studies in global markets.

This role involves study design, regulatory liaison, and collaboration with Regulatory, R&D, Medical Affairs, Quality, and Commercial teams, while mentoring junior scientists and staying current with guidelines and