Clinical Research Scientist

About Ceribell

Ceribell produces the world’s first brain monitor for point-of-care seizure triage and treatment. Our groundbreaking technology enables healthcare providers to test for a suspected seizure and then deliver treatments within minutes.
We are a rapidly growing venture capital-backed medical technology startup. Ceribell is being used in hundreds of community hospitals, large academic facilities and major IDN’s across the country. With extensive clinical validation of the effectiveness of our product and significant growth potential, Ceribell is a fantastic career opportunity.

About the role:
The Clinical Research Scientist provides scientific and analytic expertise to support evidence generation for publications and provides input into clinical trial design, regulatory submissions, and product development support. Performs data analysis and literature searches related to clinical evidence. Collaborates with various internal stakeholders (Clinical Operations, Regulatory, Marketing, R&D) and external experts (physicians and other Key Opinion Leaders (KOLs)) to assist in clinical strategy, scientific publications, and product design.

Your responsibilities will include:

• Supporting evidence generation process from evidence gap analysis through study concept, protocol development, data collection, data analysis, and final write-up.
• Analyzing retrospective and prospective clinical study datasets to further Ceribell’s evidence generation activities.
• Authoring manuscripts and abstracts for submission and publication in peer reviewed scientific journals; and authoring slide and poster presentations for scientific meetings/congresses worldwide.
• Building and maintaining strong relationships with internal and external scientific, technical, and organizational leaders to support clinical and product strategies including study and site clinicians and investigators.
• Representing Ceribell at scientific conferences and with regulatory agencies, investigational meetings, and Advisory Boards.
• Contributing as part of the Clinical Research team to determine appropriate evaluation, interpretation, and presentation of data.

Required qualifications:

• Master’s Degree in science or biomedical engineering
• 2+ years of relevant experience in data analysis and/or clinical research
• Experience analyzing complex data and presenting it to varying levels of audience
• Experience writing peer-reviewed journal articles
• Ability (and desire) to effectively manage multiple projects in fast-paced startup environment

Preferred qualifications:

• PhD in science or biomedical engineering
• Background in biostatistics, public health, data science, experimental psychology, neuroscience, or related field
• Experience with industry data analytics, healthcare data, and/or neurology
• Medical device experience, especially diagnostic or AI devices
• Clinical trial or clinical data study design experience
• Published first author of peer-reviewed journal articles