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Salary: USD 168,000 - 185,000 / annual
Ceribell is a medical technology company transforming the diagnosis and management of serious neurological conditions through its point-of-care EEG platform deployed across hundreds of community hospitals and academic facilities nationwide.
The Principal Clinical Research Scientist owns the full lifecycle of clinical evidence generation—from gap analysis and literature review through study conception, protocol development, data collection, analysis, manuscript authorship, and peer-reviewed publication. You will author and present scientific communications (abstracts, manuscripts, posters, presentations) for peer-reviewed and commercial audiences at major scientific conferences and congresses.
Key responsibilities include:
- Managing the clinical evidence library and publication pipeline, coordinating timelines with Regulatory and Marketing teams
- Supporting regulatory submissions with clinical evidence and trial results (e.g., FDA 510(k))
- Contributing to the design of prospective and retrospective clinical studies on existing and future products
- Interfacing with study investigators, KOL advisors, and internal teams (Data Science, Regulatory, Marketing, Product)
- Maintaining strong relationships with clinical and scientific leaders to advance study execution and results dissemination
- Developing and executing conference activities for major medical meetings, including abstract submissions, KOL engagement, and investigator coordination
- Partnering with Marketing, Sales, and Go-to-Market teams to develop clinical evidence summaries, infographics, and data visualizations while ensuring scientific integrity, data accuracy, and regulatory compliance
You will translate complex clinical data for diverse audiences—clinicians, regulators, and commercial teams—and work closely with clinical operations, regulatory, marketing, R&D, and external experts to drive adoption and support clinical decision-making.
REQUIREMENTS:
- 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 demonstrated 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
PREFERRED QUALIFICATIONS:
- 8+ years of clinical research experience in the medical device industry
- Neuroscience expertise
- Clinical trial or clinical data study design experience
