Remote Senior Clinical Scientist - Trials & Regulatory

Danaher Corporation; Miami (FL); Remote; USD 130,000 - 150,000; Full time

Benefits offered by this job

Paid time off

Medical insurance

Dental insurance

Vision insurance

401(k)

Job summary

Beckman Coulter Diagnostics, a Danaher operating company, is seeking a Principal Clinical Scientist to lead clinical trial strategies in the US and EU. Based in Miami with remote work options, you will collaborate across Regulatory, R&D, and Medical Affairs to drive evidence generation and submissions.

You will design studies, liaise with regulatory bodies, and author critical trial documentation while mentoring junior scientists and advancing diagnostic technology.

Qualifications

• Bachelor’s degree in Life Sciences with 9+ years of clinical research experience.
• Experience with US and/or EU regulatory trials in diagnostics or medical devices.
• Strong communication and interpersonal skills for cross-functional collaboration.

Responsibilities

• Design clinical studies and evidence strategies for global regulatory submissions (FDA/CE).
• Act as a scientific liaison with regulatory bodies and external sites.
• Collaborate with R&D, Regulatory, Medical Affairs and Quality to align programs.
• Prepare and review study reports, technical files, and publications to support clearance and commercialization.
• Mentor junior scientists and stay updated on regulatory standards and diagnostics technology.

Skills

Clinical trial design

Regulatory strategy

Regulatory submissions

Cross-functional collaboration

Scientific communication

Education

Bachelor's degree in Life Sciences

Master's degree (preferred)

Doctoral degree (advantage)

Job description

Beckman Coulter Diagnostics, a Danaher operating company, is seeking a Principal Clinical Scientist to lead clinical trial strategies in the US and EU. Based in Miami with remote work options, you will collaborate across Regulatory, R&D, and Medical Affairs to drive evidence generation and submissions.

You will design studies, liaise with regulatory bodies, and author critical trial documentation while mentoring junior scientists and advancing diagnostic technology.