Manager, Strategic Clinical Research

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!

• →Translate research concepts and evidence gaps into well-defined research questions, robust protocols, and actionable study plans aligned with the clinical evidence strategy. Collaborate with internal teams and external stakeholders, including study investigators, to refine research concepts and develop feasible, fit-for-purpose study designs with scientific rigor appropriate to the research question and objectives.
• →Conduct literature reviews to evaluate the existing evidence base, identify research gaps, and inform study design, endpoints, and methodology.
• →Manage the planning and development of a portfolio of research projects, tracking milestones, dependencies, and deliverables while proactively escalating risks or decisions requiring leadership input. 
• →Lead or contribute to the analysis, interpretation, and dissemination of study data, in collaboration with research scientists and external statisticians, as appropriate.
• →Partner with Commercial/Go-To-Market, Marketing, and other cross-functional teams to translate research findings into scientifically-accurate product messaging and commercial materials.
• →Other responsibilities as assigned by your Manager/Supervisor 

• Advanced degree (Ph.D., M.A./M.S., M.D., Pharm.D., or equivalent) in a scientific or clinical field, with formal training or demonstrated expertise in clinical research methodology (such as Clinical Research, Epidemiology, Public Health, Biostatistics, or related discipline)
• 7+ years of clinical research experience, with 5+ years in the medical device or pharmaceutical industry, and demonstrated success advancing projects from study design and development through execution, analysis, and reporting
• Strong knowledge of clinical research design, protocol development, and statistical methods sufficient to inform rigorous study design across varied methodologies.
• Strong organizational skills and demonstrated ability to independently manage multiple projects, proactively resolve ambiguity, mitigate risks, and drive deliverables forward with limited oversight.

• Experience in electronic health record (EHR) data, real-world evidence (RWE), and/or neurology, pediatric, or neonatal research is highly desirable
• Experience with clinical research involving AI-enabled medical devices or SaMD is a plus