Remote Principal Clinical Scientist, Diagnostics

Beckman Coulter Diagnostics; Pittsburgh (Allegheny County); Remote; USD 120,000 - 130,000; Full time

Benefits offered by this job

Bonus/incentive pay

Remote work options

Competitive benefits

Job summary

Beckman Coulter Diagnostics, part of Danaher Diagnostics, seeks a Principal Clinical Scientist to lead global trial design and regulatory strategy for US/EU markets. The role combines scientific leadership with regulatory execution and cross‑functional collaboration.

You will drive study design, partner with R&D, Medical Affairs and Quality, and prepare robust evidence packages to support product clearance and commercialization.

Qualifications

• Bachelor’s degree in Life Sciences with extensive experience in US/EU trials.
• Proven ability to design studies and interpret clinical data for regulatory submissions.
• Experience communicating with regulators and cross‑functional teams.

Responsibilities

• Design clinical studies and evidence strategies supporting global regulatory submissions.
• Act as a scientific liaison with regulatory bodies, key opinion leaders, and sites.
• Partner cross‑functionally to align clinical programs with product development needs.
• Author and review clinical/regulatory documentation to support clearance.
• Mentor junior scientists and stay updated on evolving regulatory standards.

Skills

Clinical study design

Regulatory submissions

Cross-functional collaboration

Scientific writing

External stakeholder liaison

Education

Bachelor's degree in Life Sciences, Healthcare, or related field

Master’s degree in Life Sciences, Regulatory/Clinical Affairs or related field

Doctoral degree in Life Sciences or related field

Job description

Beckman Coulter Diagnostics, part of Danaher Diagnostics, seeks a Principal Clinical Scientist to lead global trial design and regulatory strategy for US/EU markets. The role combines scientific leadership with regulatory execution and cross‑functional collaboration.

You will drive study design, partner with R&D, Medical Affairs and Quality, and prepare robust evidence packages to support product clearance and commercialization.