Principal Clinical Research Scientist (Hybrid)

United States·Sunnyvalelead

Data ScientistData

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Quick Summary

Key Responsibilities

Own the full lifecycle of clinical evidence generation from gap analysis through literature review, study conception, protocol development, data collection and analysis,

Requirements Summary

8+ years of clinical research experience in the medical device industry Neuroscience expertise Clinical trial or clinical data study design experience To complete your application,

Technical Tools

Data ScientistData

Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. The Ceribell System is a novel, point-of-care electroencephalography (“EEG”) platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. Our entire team is driven by a shared commitment to transforming the landscape of critical care through our rapid seizure detection technology, come join the movement!

Responsibilities

~1 min read

→Own the full lifecycle of clinical evidence generation from gap analysis through literature review, study conception, protocol development, data collection and analysis, to manuscript authorship and publication in peer-reviewed journals.
→Authoring and presenting scientific communications (abstracts, manuscripts, posters, presentations) for peer-reviewed and commercial audiences at scientific conferences and congresses.
→Managing the clinical evidence library and publication pipeline, maintaining timelines and coordinating with Regulatory and Marketing on publication and presentation strategy.
→Supporting regulatory submissions with clinical evidence and results from clinical trials (e.g. FDA 510(k)).
→Contribute to the design of prospective and retrospective clinical studies on existing and future products, and interface with study investigators, KOL advisors, and internal teams (Data Science, Regulatory, Marketing, Product).
→Maintaining strong relationships with clinical and scientific leaders (site investigators, principal investigators, KOL advisors) to advance study execution, analysis and results dissemination.
→Developing and executing conference activities for major medical meetings, including abstract/presentation submissions, KOL engagement, and investigator coordination.
→Work in close partnership with Marketing, Sales, and Go-to-Market teams to drive the development of clinical evidence summaries, infographics, and data visualizations, guaranteeing scientific integrity, data accuracy, and regulatory compliance.
→Other responsibilities as assigned by your Manager/Supervisor

PhD in Clinical Research, Engineering, Epidemiology, Biostatistics, Public Health, or related life science discipline
5 + years of clinical research experience in the medical device or pharmaceutical industry
Proficiency in statistical analysis (R, Python, or equivalent)
Strong scientific writing and experience writing peer-reviewed journal articles
Demonstrated ability to analyze and interpret clinical data
Excellent written and verbal communication skills; ability to translate complex clinical data for diverse audiences (clinicians, regulators, commercial teams)

Requirements

~1 min read

8+ years of clinical research experience in the medical device industry
Neuroscience expertise
Clinical trial or clinical data study design experience

Compensation Range

$168,000—$185,000 USD

A candidate’s final salary offer will be based on their skills, education, work location and experience, and thus it may differ from the posted range. Compensation may also include bonuses consistent with Ceribell’s corporate compensation plan. Note, the above description is not all-encompassing and Ceribell reserves the right to change or modify job duties and assignments at any time.