Senior Clinical Scientist - Diagnostics (Remote)

Beckman Coulter Diagnostics

Cleveland (OH)

Hybrid

USD 120,000 - 165,000

Full time

2 days ago
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Benefits offered by this job

Bonus eligible
Remote work options

Job summary

Beckman Coulter Diagnostics in the US is seeking a Principal Clinical Scientist to lead clinical trial strategies across US and EU, supporting regulatory submissions and product development. This remote-based role may be onsite in Chaska, MN.

You will design studies, act as liaison with regulators, and collaborate with R&D, Regulatory, Medical Affairs and Quality to align programs with market access needs. A strong background in life sciences with 9+ years in clinical research, plus experience

Qualifications

  • Design clinical studies and evidence strategies for global regulatory submissions (FDA/CE) across diagnostic modalities.
  • Liaise with regulators and key opinion leaders to develop protocols, claims and evidence plans.
  • Collaborate cross-functionally with R&D, Regulatory, Medical Affairs, Quality and Commercial teams.

Responsibilities

  • Design clinical studies and evidence strategies supporting regulatory submissions.
  • Act as scientific liaison with regulatory bodies and external sites.
  • Partner with cross-functional teams to align clinical programs with product development and market access needs.
  • Author and review study reports, technical files and publications for clearance and commercialization.
  • Mentor junior scientists and stay current with evolving regulatory standards.

Skills

Clinical trial design
Regulatory submissions
Cross-functional collab
Scientific writing

Education

Bachelor’s degree in Life Sciences
Master’s degree in Life Sciences
Doctoral degree (Life Sciences)

Job description

Beckman Coulter Diagnostics in the US is seeking a Principal Clinical Scientist to lead clinical trial strategies across US and EU, supporting regulatory submissions and product development. This remote-based role may be onsite in Chaska, MN.

You will design studies, act as liaison with regulators, and collaborate with R&D, Regulatory, Medical Affairs and Quality to align programs with market access needs. A strong background in life sciences with 9+ years in clinical research, plus experience

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