Principal Clinical Research Scientist (Hybrid)

<div class="content-intro"><p><strong>About Ceribell</strong></p> <p>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!</p></div><p><strong>Position Overview</strong>:</p> <p>The Principal Clinical Research Scientist is responsible for generating, analyzing, and communicating clinical evidence to support product development, regulatory submissions, and commercial growth. This individual combines strong data analysis and scientific writing skills with hands-on conference strategy and marketing activities. This role works closely with clinical operations, regulatory, marketing, R&D teams and external experts (physicians and key opinion leaders) to translate clinical data into publications, presentations, and marketing materials that drive adoption and support clinical decision-making.</p> <p><strong>What you'll do:</strong></p> <ul> <li>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.</li> <li>Authoring and presenting scientific communications (abstracts, manuscripts, posters, presentations) for peer-reviewed and commercial audiences at scientific conferences and congresses.</li> <li>Managing the clinical evidence library and publication pipeline, maintaining timelines and coordinating with Regulatory and Marketing on publication and presentation strategy.</li> <li>Supporting regulatory submissions with clinical evidence and results from clinical trials (e.g. FDA 510(k)).</li> <li>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).</li> <li>Maintaining strong relationships with clinical and scientific leaders (site investigators, principal investigators, KOL advisors) to advance study execution, analysis and results dissemination.</li> <li>Developing and executing conference activities for major medical meetings, including abstract/presentation submissions, KOL engagement, and investigator coordination.</li> <li>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.</li> <li>Other responsibilities as assigned by your Manager/Supervisor </li> </ul> <p><strong>What We're Looking For: </strong></p> <ul> <li>PhD in Clinical Research, Engineering, Epidemiology, Biostatistics, Public Health, or related life science discipline</li> <li>5 + years of clinical research experience in the medical device or pharmaceutical industry</li> <li>Proficiency in statistical analysis (R, Python, or equivalent)</li> <li>Strong scientific writing and experience writing peer-reviewed journal articles </li> <li>Demonstrated ability to analyze and interpret clinical data</li> <li>Excellent written and verbal communication skills; abi